Wayseen Wang

发表

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.

Chih-ping Chen, T. Ko, S. Chern, 2017, Taiwanese journal of obstetrics & gynecology.

Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2013, Gene.

Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Gene.

Pregnancy with de novo 9q34.3 microdeletion and Kleefstra syndrome in the fetus may be associated with an abnormal maternal serum screening result.

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2015, Taiwanese journal of obstetrics & gynecology.

3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Gene.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome.

Chih-ping Chen, T. Ko, Wayseen Wang, 2013, Gene.

An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2013, Gene.

Prenatal diagnosis of monosomy 17p (17p13.3-->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly, and Miller-Dieker lissencephaly syndrome in a fetus.

Chih-ping Chen, P. Su, Wayseen Wang, 2009, Taiwanese journal of obstetrics & gynecology.

Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2009, Taiwanese journal of obstetrics & gynecology.

Novel mutation in the TSC2 gene associated with prenatally diagnosed cardiac rhabdomyomas and cerebral tuberous sclerosis.

Chih-ping Chen, Wayseen Wang, Yidi Su, 2006, Journal of the Formosan Medical Association = Taiwan yi zhi.

Molecular genetic analysis of the TSC genes in two families with prenatally diagnosed rhabdomyomas

Chih-ping Chen, F. Hsieh, Chien-Nan Lee, 2005, Prenatal diagnosis.

Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion.

Chih-ping Chen, T. Ko, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Molecular diagnosis of a novel heterozygous 268C→T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis

Chih-ping Chen, S. Chern, Wayseen Wang, 2002, Prenatal diagnosis.

Prenatal diagnosis of de novo interstitial deletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect.

Chih-ping Chen, Ming-Chao Huang, S. Chern, 2013, Gene.

Short Communication Mosaic trisomy 2 at amniocentesis: Prenatal diagnosis and molecular genetic analysis

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2012 .

Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese journal of obstetrics & gynecology.

A paternally derived inverted duplication of distal 14q with a terminal 14q deletion

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2005, American journal of medical genetics. Part A.

Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay.

Chih-ping Chen, F. Tsai, S. Chern, 2008, European journal of medical genetics.

Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2-->q24.3 in a girl with autistic features and developmental delay.

Chih-ping Chen, F. Tsai, S. Chern, 2010, European journal of medical genetics.

Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2021, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of de novo pure partial monosomy 4p (4p15.1 → pter) in a growth‐restricted fetus with a Greek warrior helmet face and unilateral facial cleft on three‐dimensional ultrasound

Chih-ping Chen, Wayseen Wang, Wen‐Lin Chen, 2004, Prenatal diagnosis.

Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results.

Chih-ping Chen, K. Seow, S. Chern, 2020, Taiwanese journal of obstetrics & gynecology.

Partial trisomy 10q (10q25.1 →qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

NFκB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1 → qter)

Chih-ping Chen, F. Tsai, S. Chern, 2008, Prenatal diagnosis.

Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3).

Chih-ping Chen, S. Chern, H. Au, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2021, Taiwanese journal of obstetrics & gynecology.

Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defects.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2019, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound.

Chih-ping Chen, T. Ko, S. Chern, 2020, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Uncomplicated vaginal delivery in two consecutive pregnancies carried to term in a woman with osteogenesis imperfecta type I and bisphosphonate treatment before conception.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus.

Chih-ping Chen, T. Ko, S. Chern, 2021, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2018, Taiwanese journal of obstetrics & gynecology.

Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus.

Chih-ping Chen, T. Ko, S. Chern, 2018, Taiwanese journal of obstetrics & gynecology.

Short rib-polydactyly syndrome type II (Majewski): prenatal diagnosis, perinatal imaging findings and molecular analysis of the NEK1 gene.

Chih-ping Chen, F. Tsai, S. Chern, 2012, Taiwanese journal of obstetrics & gynecology.

Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2→p14).

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Gene.

Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: prenatal diagnosis and aCGH characterization using uncultured amniocytes.

Chih-ping Chen, Ming-Chao Huang, S. Chern, 2013, Gene.

Rapid detection of de novo P253R mutation in FGFR2 using uncultured amniocytes in a pregnancy affected by polyhydramnios, Blake's pouch cyst, and Apert syndrome.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele

Chih-ping Chen, F. Tsai, S. Chern, 2008, Prenatal diagnosis.

Prenatal diagnosis of premature centromere division–related mosaic variegated aneuploidy

Chih-ping Chen, C. Tzen, Wayseen Wang, 2004, Prenatal diagnosis.

Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autism and congenital heart defects.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2021, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Gene.

Prenatal diagnosis of a 1.651-Mb 19q13.42-q13.43 microdeletion in a fetus with micrognathia and bilateral pyelectasis on prenatal ultrasound.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Perinatal imaging findings of inherited Sotos syndrome

Chih-ping Chen, N. Chiu, Shuan-Pei Lin, 2002, Prenatal diagnosis.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Gene.

Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature.

Chih-ping Chen, Ming-Chao Huang, S. Chern, 2015, Taiwanese journal of obstetrics & gynecology.

Array CGH characterization of an unbalanced X-autosome translocation associated with Xq27.2-qter deletion, 11q24.3-qter duplication and Xq22.3-q27.1 duplication in a girl with primary amenorrhea and mental retardation.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2014, Gene.

A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2014, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

A false-positive result at non-invasive prenatal testing due to maternal 17p12 microduplication.

Chih-ping Chen, Peih-Shan Wu, Shin-Wen Chen, 2022, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome.

Chih-ping Chen, Wayseen Wang, Yi-Yung Chen, 2011, Taiwanese journal of obstetrics & gynecology.

Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature

Chih-ping Chen, C. Tzen, S. Chern, 2004, Prenatal diagnosis.

Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome.

Chih-ping Chen, T. Ko, S. Chern, 2020, Taiwanese journal of obstetrics & gynecology.

Perinatal cytogenetic discrepancy in a fetus with low-level mosaicism for trisomy 21 and a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes.

Chih-ping Chen, Yeou-Lih Wang, S. Chern, 2016, Taiwanese journal of obstetrics & gynecology.

Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2014, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 → pter) and partial monosomy 9p (9p22 → pter)

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2005, Prenatal diagnosis.

Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2006, American journal of medical genetics. Part A.

Discordant anencephaly and Cantrell syndrome in monozygotic twins conceived by ICSI and IVF-ET.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese journal of obstetrics & gynecology.

Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2013, Gene.

Prenatal diagnosis and management of monozygotic twins discordant for severe fetal abnormalities.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2018, Taiwanese journal of obstetrics & gynecology.

A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome.

S. Ng, Chih-ping Chen, S. Chern, 2012, European journal of medical genetics.

Prenatal diagnosis of hydrancephaly and enlarged cerebellum and cisterna magna in a fetus with thanatophoric dysplasia type II and a review of prenatal diagnosis of brain anomalies associated with thanatophoric dysplasia.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2018, Taiwanese journal of obstetrics & gynecology.

22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect: prenatal diagnosis by array comparative genomic hybridization.

Chih-ping Chen, F. Tsai, S. Chern, 2009, Taiwanese journal of obstetrics & gynecology.

Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Osteogenesis imperfecta type II: prenatal diagnosis and association with increased nuchal translucency and hypoechogenicity of the cranium.

Chih-ping Chen, Ming-Chao Huang, S. Chern, 2012, Taiwanese journal of obstetrics & gynecology.

Typical body wall defect associated with craniofacial anomalies and amniotic bands diagnosed in early pregnancy.

Chih-ping Chen, Wayseen Wang, Chin-Yuan Hsu, 2007, Taiwanese journal of obstetrics & gynecology.

Prenatal imaging findings of a rapidly involuting congenital hemangioma (RICH) over right flank in a fetus with a favorable outcome.

Chih-ping Chen, Shin-Wen Chen, Wayseen Wang, 2016, Taiwanese journal of obstetrics & gynecology.

Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Genomics.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9 p deletion and literature review

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013 .

High-level mosaicism for 45,X in 45,X/46,X,idic(Y)(q11.2) at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell line.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2022, Taiwanese journal of obstetrics & gynecology.

Perinatal cytogenetic discrepancy in a pregnancy with mosaic 45,X/46, XY at amniocentesis and a favorable outcome.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2022, Taiwanese journal of obstetrics & gynecology.

High-level mosaicism for 45,X in 45,X/46, XY at amniocentesis in a pregnancy with a favorable fetal outcome and cytogenetic discrepancy in various tissues.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2022, Taiwanese journal of obstetrics & gynecology.

Neonatal outcome of a prenatally detected 46,XX/46,XY true hermaphrodite

Chih-ping Chen, C. Tzen, Shuan-Pei Lin, 2006, Prenatal diagnosis.

Prenatal diagnosis of de novo terminal deletion of chromosome 7q

Chih-ping Chen, C. Tzen, S. Chern, 2003, Prenatal diagnosis.

Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes.

Chih-ping Chen, S. Chern, C. Pan, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal sonographic findings of Klippel‐Trénaunay‐Weber syndrome

Chih-ping Chen, Jian-Pei Huang, H. Hung, 2007, Journal of clinical ultrasound : JCU.

Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Second‐trimester evaluation of fetal sacrococcygeal teratoma using three‐dimensional color Doppler ultrasound and magnetic resonance imaging

Chih-ping Chen, C. Tzen, Wayseen Wang, 2003, Prenatal diagnosis.

Second‐trimester magnetic resonance imaging of fetal sacrococcygeal teratoma with intrapelvic extension in a co‐twin

Chih-ping Chen, C. Tzen, Wayseen Wang, 2004, Prenatal diagnosis.

Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review.

Wan-Yuo Guo, Li-Feng Chen, Chih-ping Chen, 2013, Gene.

Ventriculomegaly, intrauterine growth restriction, and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2 --> pter) in a fetus.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2010, Taiwanese journal of obstetrics & gynecology.

Ring chromosome 21 presenting with sacrococcygeal teratoma: prenatal diagnosis, molecular cytogenetic characterization and literature review.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Gene.

Prenatal diagnosis of cystic bladder distension secondary to obstructive uropathy

Chih-ping Chen, C. Tzen, Wayseen Wang, 2000, Prenatal diagnosis.

Balanced reciprocal translocations detected at amniocentesis.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2005, Prenatal diagnosis.

Detection of hypomethylation of H19 in a pregnancy with limb-body wall complex.

Chih-ping Chen, Ming-Chao Huang, S. Chern, 2018, Taiwanese journal of obstetrics & gynecology.

Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2013, Gene.

Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth.

Chih-ping Chen, Wayseen Wang, Chih-Ping Chen, 2013, Taiwanese journal of obstetrics & gynecology.

6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and developmental delay.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2013, Gene.

Prenatal diagnosis of low‐level mosaic tetrasomy 9p by amniocentesis

Chih-ping Chen, S. Chern, Wayseen Wang, 2007, Prenatal diagnosis.

Prenatal diagnosis of low‐level mosaic trisomy 7 by amniocentesis

Chih-ping Chen, S. Chern, Wayseen Wang, 2005, Prenatal diagnosis.

Rapid confirmation of trisomy 13 of maternal origin by QF-PCR following postmortem tissue cell culture failure in a pregnancy with trisomy 13 at amniocentesis and fetal postaxial polydactyly and facial cleft.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2022, Taiwanese journal of obstetrics & gynecology.

Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2009, Taiwanese journal of obstetrics & gynecology.

OMPHALOCELE IN A MALE FETUS: PRENATAL MAGNETIC RESONANCE IMAGING FINDINGS AND LITERATURE REVIEW

Chih-ping Chen, F. Tsai, Wayseen Wang, 2009 .

First-trimester two-dimensional and three-dimensional ultrasound demonstration of craniofacial defects, abdominal wall defects and upper limb deficiency associated with limb-body wall complex.

Chih-ping Chen, Wayseen Wang, Yi-Yung Chen, 2011, Taiwanese journal of obstetrics & gynecology.

Limb-body wall complex in one fetus of a dizygotic twin pregnancy conceived by egg donation, in vitro fertilization and embryo transfer: prenatal diagnosis and literature review.

Chih-ping Chen, Ming-Chao Huang, F. Tsai, 2009, Taiwanese journal of obstetrics & gynecology.

Prenatal 3‐dimensional sonographic and MRI findings in omphalocele–exstrophy–imperforate anus–spinal defects complex

Chih-ping Chen, F. Tsai, Wayseen Wang, 2008, Journal of clinical ultrasound : JCU.

Prenatal ultrasound demonstration of limb-body wall complex with megacystis.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Limb-body wall complex with craniofacial defects after ovarian stimulation.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2008, Taiwanese journal of obstetrics & gynecology.

Prenatal imaging of limb‐body wall complex by magnetic resonance imaging

Chih-ping Chen, Sho-Jen Cheng, Wayseen Wang, 2005, Prenatal diagnosis.

Prenatal Diagnosis of LimbeBody Wall Complex With Craniofacial Defects

Chih-ping Chen, Wayseen Wang, Yi-Yung Chen, 2022 .

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15).

Chih-ping Chen, S. Chern, Hsiang-Yu Lin, 2020, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2014, Taiwanese journal of obstetrics & gynecology.

Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1→qter) and partial monosomy 20q (20q13.3→qter)

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2005, Prenatal diagnosis.

Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements

Chih-ping Chen, S. Chern, Wayseen Wang, 2006, Prenatal diagnosis.

Prenatal diagnosis of partial trisomy 16q and distal 22q13 deletion associated with dolichocephaly and frontal bossing on second‐trimester ultrasound

Chih-ping Chen, Wayseen Wang, Wen‐Lin Chen, 2005, Prenatal diagnosis.

Prenatal diagnosis of complete trisomy 16q in two consecutive pregnancies

Chih-ping Chen, Wayseen Wang, Chen‐Chi Lee, 2004, Prenatal diagnosis.

Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2003, Prenatal diagnosis.

Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation.

Chih-ping Chen, F. Tsai, S. Chern, 2008, Fertility and sterility.

Prenatal diagnosis of an interstitial deletion of 10q (10q11.21 → q21.1): array comparative genomic hybridization characterization and literature review.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→qter)

Chih-ping Chen, S. Chern, Wayseen Wang, 2006, Prenatal diagnosis.

Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.

Chih-ping Chen, Wayseen Wang, Chen‐Chi Lee, 2006, Fertility and sterility.

Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1.

Chih-ping Chen, Chih-heng Hsieh, S. Chern, 2017, Taiwanese journal of obstetrics & gynecology.

Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2014, Taiwanese journal of obstetrics & gynecology.

Cytogenetic variability in the proportion of abnormal cells between the various tissues in prenatally detected mosaic tetrasomy 12p

Chih-ping Chen, F. Tsai, S. Chern, 2007, Prenatal diagnosis.

De novo duplication of Xq22.1→q24 with a disruption of the NXF gene cluster in a mentally retarded woman with short stature and premature ovarian failure.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of congenital chylothorax associated with de novopartial trisomy 12q (12q21.2→qter)

Chih-ping Chen, C. Tzen, S. Chern, 2006, Prenatal diagnosis.

Wolf-Hirschhorn syndrome: Prenatal diagnosis and molecular cytogenetic characterization of a de novo distal deletion of 4p (4p16.1 → pter) in a fetus with facial cleft and preaxial polydactyly.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer.

Chih-ping Chen, S. Chern, Shee-Uan Chen, 2014, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of persistent left superior vena cava, polyhydramnios and a small gastric bubble in a fetus with VACTERL association.

Chih-ping Chen, Shin-Wen Chen, Wayseen Wang, 2021, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.

Chih-ping Chen, F. Tsai, T. Ko, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2018, Taiwanese journal of obstetrics & gynecology.

First-trimester prenatal diagnosis of Ellis-van Creveld syndrome.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

First-trimester prenatal diagnosis of Ellisevan Creveld syndrome

Chih-ping Chen, S. Chern, Wayseen Wang, 2012 .

VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal ultrasound demonstration of scoliosis, absence of one rib, a radial club hand, congenital heart defects and absent stomach in a fetus with VACTERL association.

Chih-ping Chen, Ming-Chao Huang, S. Chern, 2012, Taiwanese journal of obstetrics & gynecology.

Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma.

Chih-ping Chen, Ming-Chao Huang, T. Ko, 2015, Taiwanese journal of obstetrics & gynecology.

Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.

Chih-ping Chen, F. Tsai, S. Chern, 2009, Taiwanese Journal of Obstetrics & Gynecology.

REARRANGEMENTS INVOLVING CHROMOSOMES OTHER THAN CHROMOSOME 21

Chih-ping Chen, F. Tsai, S. Chern, 2009 .

Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia.

Chih-ping Chen, S. Chern, Wayseen Wang, 2014, Taiwanese journal of obstetrics & gynecology.

Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma, and intrauterine growth restriction.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

First-trimester molecular diagnosis of complete hydatidiform mole associated with dizygotic twin pregnancy conceived by intrauterine insemination.

Chih-ping Chen, T. Ko, S. Chern, 2014, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 14 at amniocentesis: prenatal diagnosis and literature review.

Chih-ping Chen, T. Ko, S. Chern, 2013, Taiwanese journal of obstetrics & gynecology.

Detection of balanced homologous acrocentric rearrangement rea(14q14q) and low-grade X-chromosome mosaicism in a couple with repeated pregnancy losses.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 21 at amniocentesis in a twin pregnancy associated with a favorable fetal outcome, maternal uniparental disomy 21 and postnatal decrease of the trisomy 21 cell line.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2023, Taiwanese Journal of Obstetrics & Gynecology.

Prenatal diagnosis of mosaicism for double aneuploidy of 47,XXY and trisomy 7 (48,XXY,+7) at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2021, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction

Chih-ping Chen, C. Tzen, S. Chern, 2003, Prenatal diagnosis.

Digynic triploidy in a fetus presenting with semilobar holoprosencephaly.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2018, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

First-trimester sonographic demonstration of digynic triploidy.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly.

Chih-ping Chen, F. Tsai, S. Chern, 2009, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency

Chih-ping Chen, S. Chern, Wayseen Wang, 2005, Prenatal diagnosis.

Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization, and literature review.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2014, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of trisomy 11 in a single colony of cultured amniocytes at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2021, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaicism for trisomy 12 in a single colony at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaicism for double trisomies of trisomy 11 and trisomy 12 in a single colony at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaicism for trisomy 11 in a single colony at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Weng, S. Chern, 2020, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Rapid genome-wide aneuploidy diagnosis using uncultured amniocytes and array comparative genomic hybridization in pregnancy with abnormal ultrasound findings detected in late second and third trimesters.

Chih-ping Chen, Ming-Chao Huang, F. Tsai, 2010, Taiwanese journal of obstetrics & gynecology.

Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of trisomy 8 mosaicism.

Chih-ping Chen, S. Chern, C. Pan, 2012, Taiwanese journal of obstetrics & gynecology.

Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic trisomy 9.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of low‐level mosaic trisomy 6 by amniocentesis

Chih-ping Chen, S. Chern, Wayseen Wang, 2006, Prenatal diagnosis.

Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha‐fetoprotein and human chorionic gonadotrophin

Chih-ping Chen, S. Chern, Wayseen Wang, 2004, Prenatal diagnosis.

Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4

Chih-ping Chen, C. Tzen, S. Chern, 2004, Prenatal diagnosis.

Fetoplacental and fetoamniotic chromosomal discrepancies in prenatally detected mosaic trisomy 9

Chih-ping Chen, S. Chern, Wayseen Wang, 2003, Prenatal diagnosis.

Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2022, Taiwanese journal of obstetrics & gynecology.

Unbalanced and balanced heterologous acrocentric rearrangements involving chromosome 21 at amniocentesis.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21).

Chih-ping Chen, T. Ko, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3.

Chih-ping Chen, T. Ko, S. Chern, 2019, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of pseudomosaicism for trisomy 20 at amniocentesis with a negative non-invasive prenatal testing (NIPT) result in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2022, Taiwanese journal of obstetrics & gynecology.

Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic 46,XX,dup(9)(q22.3q34.1)/46,XX at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2022, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of maternal uniparental disomy 21 in association with low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2022, Taiwanese journal of obstetrics & gynecology.

Second‐trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature

Chih-ping Chen, C. Tzen, Sho-Jen Cheng, 2004, Prenatal diagnosis.

Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic trisomy 16 by amniocentesis in a pregnancy associated with abnormal first-trimester screening result (low PAPP-A and low PlGF), intrauterine growth restriction and a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2021, Taiwanese journal of obstetrics & gynecology.

Unbalanced reciprocal translocations at amniocentesis.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2019, Taiwanese journal of obstetrics & gynecology.

Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2)

Chih-ping Chen, S. Chern, Wayseen Wang, 1999, Prenatal diagnosis.

A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1

Chih-ping Chen, C. Tzen, S. Chern, 2007, Prenatal diagnosis.

Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling.

Chih-ping Chen, Ming-Chao Huang, F. Tsai, 2010, Taiwanese journal of obstetrics & gynecology.

Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3→q31.3) associated with Gorlin syndrome

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2006, Prenatal diagnosis.

Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2020, Taiwanese journal of obstetrics & gynecology.

Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: prenatal diagnosis and literature review.

Chih-ping Chen, Wayseen Wang, Yidi Su, 2013, Taiwanese journal of obstetrics & gynecology.

Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review.

Chih-ping Chen, F. Tsai, S. Chern, 2008, Fertility and sterility.

Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2006, Prenatal diagnosis.

Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion

Chih-ping Chen, C. Tzen, S. Chern, 2003, Prenatal diagnosis.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 2q12.2→q13 encompassing MALL, NPHP1, RGPD6 and BUB1.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2022, Taiwanese journal of obstetrics & gynecology.

Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2017, Taiwanese journal of obstetrics & gynecology.

Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2019, Taiwanese journal of obstetrics & gynecology.

Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.

Late-onset fetal bilateral pleural effusions associated with Down syndrome.

Chih-ping Chen, Peih-Shan Wu, C. Pan, 2018, Taiwanese journal of obstetrics & gynecology.

Prenatal sonography and magnetic resonance imaging of pulmonary sequestration associated with a gastric duplication cyst

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2006, Prenatal diagnosis.

Prenatal magnetic resonance imaging demonstration of the systemic feeding artery of a pulmonary sequestration associated with in utero regression

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2005, Prenatal diagnosis.

Prenatal diagnosis of right pulmonary agenesis associated with VACTERL sequence

Chih-ping Chen, Wayseen Wang, Yi-Hui Lin, 2003, Prenatal diagnosis.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly

Chih-ping Chen, S. Chern, Wayseen Wang, 2001, Prenatal diagnosis.

Prenatal Two- and Three-Dimensional Ultrasound Diagnosis of Limb Reduction Defects Associated with Homozygous α-Thalassemia

Chih-ping Chen, Wayseen Wang, Yidi Su, 2006, Fetal Diagnosis and Therapy.

Recurrent short‐rib polydactyly syndrome: prenatal three‐dimensional ultrasound findings and associations with congenital high airway obstruction and pyelectasia

Chih-ping Chen, C. Tzen, Wayseen Wang, 2005, Prenatal diagnosis.

Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3→qter) and partial trisomy 18q (18q23→qter) in a fetus associated with cystic hygroma and ambiguous genitalia

Chih-ping Chen, T. Ko, S. Chern, 2005, Prenatal diagnosis.

Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes.

Chih-ping Chen, F. Tsai, Shuan-Pei Lin, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia.

Chih-ping Chen, Yeou-Lih Wang, S. Chern, 2015, Taiwanese journal of obstetrics & gynecology.

Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of maternal epilepsy.

Wan-Yuo Guo, Chih-ping Chen, S. Chern, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of a fetus with distal 10q trisomy

Chih-ping Chen, Wayseen Wang, Tao‐Yeuan Wang, 1999, Prenatal diagnosis.

A 12 Mb deletion of 6p24.1-->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys.

Chih-ping Chen, C. Tzen, F. Tsai, 2009, European journal of medical genetics.

Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism.

Chih-ping Chen, S. Chern, C. Pan, 2015, Taiwanese journal of obstetrics & gynecology.

Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, T. Ko, S. Chern, 2017, Taiwanese journal of obstetrics & gynecology.

Asymmetrical terminal limb defects in a hydropic infant with homozygous α‐thalassemia‐1

Chih-ping Chen, Jian-Pei Huang, Wayseen Wang, 2005, Prenatal diagnosis.

Low-level mosaicism for trisomy 16 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2021, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly.

Chih-ping Chen, Wan-Yuo Guo, Peih-Shan Wu, 2015, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2014, Taiwanese journal of obstetrics & gynecology.

Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal sonographic diagnosis of acrania associated with amniotic bands

Chih-ping Chen, Wayseen Wang, Yi-Hui Lin, 2004, Journal of clinical ultrasound : JCU.

Apert syndrome associated with upper airway obstruction and gastroesophageal reflux inducing polyhydramnios in the third trimester.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction.

Chih-ping Chen, T. Ko, S. Chern, 2016, Taiwanese journal of obstetrics & gynecology.

Rapid Aneuploidy Diagnosis by Array Comparative Genomic Hybridization Using Uncultured Amniocytes in a Pregnancy With Fetal Nuchal Edema and Mild Ascites

Chih-ping Chen, C. Pan, Wayseen Wang, 2011 .

Terminal 2q deletion and distal 15q duplication: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes.

Chih-ping Chen, F. Tsai, S. Chern, 2009, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of 46,XX,DER(13;21)(Q10;Q10),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites.

Chih-ping Chen, F. Tsai, S. Chern, 2009, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of low‐level mosaicism for a small XIST‐negative supernumerary ring X chromosome in a nondysmorphic male fetus

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2006, Prenatal diagnosis.

Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2015, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of the Dandy‐Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion

Chih-ping Chen, C. Tzen, Shuan-Pei Lin, 2002, Prenatal diagnosis.

Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2022, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Association of partial trisomy 9 (9pter→q22.3) with corpus callosum dysgenesis, bilateral subependymal cysts, and ventriculomegaly

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2003, Prenatal diagnosis.

Perinatal findings of partial trisomy 13q (13q14.1→qter) resulting from paternal pericentric inversion of chromosome 13

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2005, Prenatal diagnosis.

Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of inherited satellited non‐acrocentric chromosomes

K. Devriendt, Chih-ping Chen, S. Chern, 2000, Prenatal diagnosis.

Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2017, Taiwanese journal of obstetrics & gynecology.

Female pseudohermaphroditism in a prenatally diagnosed cloacal malformation with hydronephrosis, dilated bladder, hydrometrocolpos, and oligohydramnios.

Chih-ping Chen, Wayseen Wang, Jun-Wei Su, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia

Chih-ping Chen, C. Tzen, S. Chern, 2001, Prenatal diagnosis.

Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs, and thanatophoric dysplasia type II.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Third-trimester 3D ultrasound evaluation of thanatophoric dysplasia type I.

Chih-ping Chen, S. Chern, Wayseen Wang, 2007, Taiwanese journal of obstetrics & gynecology.

Second trimester molecular diagnosis of a stop codon FGFR3 mutation in a type I thanatophoric dysplasia fetus following abnormal ultrasound findings

Chih-ping Chen, C. Tzen, S. Chern, 2002, Prenatal diagnosis.

Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2012, Taiwanese journal of obstetrics & gynecology.

Osteogenesis imperfecta type I: second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the paucisymptomatic father.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Second‐trimester sonographic detection of short rib–polydactyly syndrome type II (Majewski) following an abnormal maternal serum biochemical screening result

Chih-ping Chen, C. Tzen, Wayseen Wang, 2003, Prenatal diagnosis.

Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p.

Chih-ping Chen, T. Ko, S. Chern, 2014, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic tetrasomy 18p.

Chih-ping Chen, T. Ko, S. Chern, 2012, Taiwanese journal of obstetrics & gynecology.

Detection of paternal origin of fetal trisomy 21 in a pregnancy with isolated ventriculomegaly but without advanced parental age.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2020, Taiwanese journal of obstetrics & gynecology.

Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndrome.

Chih-ping Chen, Chien-Hsing Lin, S. Chern, 2021, Taiwanese Journal of Obstetrics & Gynecology.

Prenatal diagnosis of mosaic ring chromosome 9

Chih-ping Chen, Wayseen Wang, Chen‐Chi Lee, 2006, Prenatal diagnosis.

Perinatal Magnetic Resonance Imaging Demonstration of Duplication of the Right Renal Collecting System with Ipsilateral Hydronephrosis and Hydroureter, and Contralateral Renal Hypoplasia

Chih-ping Chen, Wayseen Wang, Jun-Wei Su, 2011 .

Favourable outcome in a pregnancy with concomitant maternal and fetal osteogenesis imperfecta associated with a novel COL1A2 mutation

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2006, Prenatal diagnosis.

Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.

Chih-ping Chen, T. Ko, S. Chern, 2016, Taiwanese journal of obstetrics & gynecology.

Bilateral calcified ovarian fibromas in a patient with Sotos syndrome.

Chih-Long Chang, Chih-ping Chen, Yuh‐Cheng Yang, 2002, Fertility and sterility.

Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2019, Taiwanese journal of obstetrics & gynecology.

Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2010, Taiwanese journal of obstetrics & gynecology.

Detection of paternal origin of fetal de novo rea(21q;21q) down syndrome in a pregnancy of a young woman associated with an abnormal first-trimester maternal serum screening result.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2022, Taiwanese journal of obstetrics & gynecology.

Detection of mosaic balanced homologous acrocentric rearrangement rea(21q21q) in a woman with repeated pregnancy losses.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis.

Chih-ping Chen, F. Tsai, S. Chern, 2009, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2015, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome.

Chih-ping Chen, T. Ko, S. Chern, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of partial monosomy 18p(18p11.2→pter) and trisomy 21q(21q22.3→qter) with alobar holoprosencephaly and premaxillary agenesis

Chih-ping Chen, C. Tzen, S. Chern, 2001, Prenatal diagnosis.

Prenatal diagnosis of mosaic ring chromosome 4

Chih-ping Chen, C. Tzen, Wayseen Wang, 2007, Prenatal diagnosis.

A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbows.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2018, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese Journal of Obstetrics & Gynecology.

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2016, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2016, Taiwanese journal of obstetrics & gynecology.

Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasi

Chih-ping Chen, S. Chern, C. Pan, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.

Pure partial monosomy 3p (3p25.3 → pter): prenatal diagnosis and array comparative genomic hybridization characterization.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2021, Taiwanese journal of obstetrics & gynecology.

Detection of paternal origin of fetal trisomy 18 in a pregnancy conceived by assisted reproductive technology and in vitro fertilization.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2014, Gene.

Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization.

Chih-ping Chen, T. Ko, S. Chern, 2019, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1→q31.1).

Chih-ping Chen, Shing-Jyh Chang, S. Chern, 2013, Gene.

Prenatal diagnosis of mosaicism for a distal 5p deletion in a single colony at amniocentesis in a pregnancy with a favorable outcome and a review of mosaic distal 5p deletion.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts

Chih-ping Chen, C. Tzen, S. Chern, 2001, Prenatal diagnosis.

Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosomes.

Chih-ping Chen, T. Ko, Wayseen Wang, 2013, Journal of the Chinese Medical Association : JCMA.

Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2012, Taiwanese journal of obstetrics & gynecology.

Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial duplication of Yq (Yq11.2→qter) and partial monosomy 5p (5p15.3→pter)

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2005, Prenatal diagnosis.

Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of a familial Y long-arm and chromosome 15 short-arm translocation inherited from a mother carrier.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2021, Taiwanese journal of obstetrics & gynecology.

Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese Journal of Obstetrics & Gynecology.

Persistent cloaca presenting with a perineal cyst: Prenatal ultrasound and magnetic resonance imaging findings.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2012, Journal of the Chinese Medical Association.

Mosaic isochromosome 20q at amniocentesis: Prenatal diagnosis, genetic counseling and literature review.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2019, Taiwanese journal of obstetrics & gynecology.

Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2015, Taiwanese journal of obstetrics & gynecology.

Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.

Mosaic isochromosome 20q detected at amniocentesis: a likely cell culture artifact.

Chih-ping Chen, Wayseen Wang, Jun-Wei Su, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2010, Taiwanese journal of obstetrics & gynecology.

Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification using uncultured amniocytes in pregnancy with major fetal structural abnormalities.

Chih-Long Chang, Chih-ping Chen, S. Chern, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of pure distal 18q deletion

Chih-ping Chen, C. Tzen, S. Chern, 2006, Prenatal diagnosis.

Trisomy 13 mosaicism associated with cyclopia and cystic hygroma.

Chih-ping Chen, F. Tsai, S. Chern, 2009, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

First-trimester cystic hygroma and omphalocele in a fetus with Turner syndrome.

Chih-ping Chen, Shin-Wen Chen, Wayseen Wang, 2018, Taiwanese journal of obstetrics & gynecology.

Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a favorable fetal outcome and cytogenetic discrepancy in various tissues.

Chih-ping Chen, S. Weng, Peih-Shan Wu, 2023, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism.

Chih-ping Chen, F. Tsai, S. Chern, 2009, Taiwanese journal of obstetrics & gynecology.

Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic distal 5p deletion and review of the literature

Chih-ping Chen, Wayseen Wang, Tung-Yao Chang, 2004, Prenatal diagnosis.

Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes

Chih-ping Chen, C. Tzen, Wayseen Wang, 2005, Prenatal diagnosis.

Conjoined twins detected in the first trimester: a review.

Chih-ping Chen, Wayseen Wang, Jun-Wei Su, 2011, Taiwanese journal of obstetrics & gynecology.

Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31 →qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Magnetic resonance imaging demonstration of sirenomelia in one fetus of a dizygotic twin pregnancy conceived by intracytoplasmic sperm injection, in vitro fertilization and embryo transfer.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese journal of obstetrics & gynecology.

Magnetic resonance imaging demonstration of sirenomelia in one fetus of a dizygotic twin pregnancy conceived by intracytoplasmic sperm injection, invitro fertilization and embryo transfer

Chih-ping Chen, F. Tsai, S. Chern, 2022 .

Incidental Detection of Thoracoomphalopagus at Amniocentesis in a Twin Pregnancy

Chih-ping Chen, Wayseen Wang, Jun-Wei Su, 2013 .

Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 15q24 microdeletion.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese Journal of Obstetrics & Gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasia.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findings.

Chih-ping Chen, F. Tsai, Shuan-Pei Lin, 2011, Taiwanese journal of obstetrics & gynecology.

Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome.

Chih-ping Chen, Jian-Pei Huang, F. Tsai, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2018, Taiwanese journal of obstetrics & gynecology.

Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicism.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of recurrent mosaic ring chromosome 13 of maternal origin.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2021, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome.

Chih-ping Chen, T. Ko, S. Chern, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of the hypoplastic right heart syndrome with sex chromosome pentasomy (49,XXXXY)

Chih-ping Chen, C. Tzen, S. Chern, 2007, Prenatal diagnosis.

Prenatal Diagnosis of Cerebral Tubers by Magnetic Resonance Imaging Following Detection of Cardiac Rhabdomyomas by Prenatal Ultrasound in a Fetus With a Nonsense Mutation in the TSC2 gene

Chih-ping Chen, Wayseen Wang, Yidi Su, 2011 .

Contribution of ultrafast magnetic resonance imaging in prenatal diagnosis of sonographically undetected cerebral tuberous sclerosis associated with cardiac rhabdomyomas

Chih-ping Chen, N. Chiu, Wayseen Wang, 2005, Prenatal diagnosis.

A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error

Chih-ping Chen, F. Tsai, S. Chern, 2005, Prenatal diagnosis.

Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese journal of obstetrics & gynecology.

Abnormally flat facial profile on two- and three-dimensional ultrasound and array comparative genomic hybridization for the diagnosis of Pallister-Killian syndrome.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Gene.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1 → pter) and 14q (14q32.31 → qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: prenatal diagnosis and molecular cytogenetic characterization.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.

Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations.

Chih-Long Chang, Chih-ping Chen, Yeou-Lih Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Monozygotic twins discordant for low-level mosaic trisomy 17 at amniocentesis in a pregnancy with a favorable outcome and a literature review of heterokaryotypic monozygotic twins at amniocentesis.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Impact of Second-Trimester Maternal Serum Screening on Prenatal Diagnosis of Down Syndrome and the use of Amniocentesis in the Taiwanese Population

Chih-ping Chen, Wayseen Wang, Chen‐Ju Lin, 2005 .

Low-level mosaic double trisomy involving trisomy 6 and trisomy 20 (48,XY,+6,+20) at amniocentesis without uniparental disomy (UPD) 6 and UPD 20 in a pregnancy associated with a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2023, Taiwanese Journal of Obstetrics & Gynecology.

Low-level mosaic trisomy 15 at amniocentesis without uniparental disomy 15 in a pregnancy associated with cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes, a favorable fetal outcome and perinatal decrease of the aneuploid cell line.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2023, Taiwanese journal of obstetrics & gynecology.

Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis.

Chih-ping Chen, T. Ko, S. Chern, 2020, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2019, Taiwanese Journal of Obstetrics & Gynecology.

Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis.

Chih-ping Chen, Shing-Jyh Chang, S. Chern, 2016, Taiwanese Journal of Obstetrics & Gynecology.

Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, Tze‐Chien Chen, T. Ko, 2022, Taiwanese journal of obstetrics & gynecology.

Research Letter Prenatal diagnosis of mosaic trisomy 9

Chih-ping Chen, S. Chern, Wayseen Wang, 2011 .

Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2022, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy‐Walker variant and trigonocephaly

Chih-ping Chen, C. Tzen, Wayseen Wang, 2002, Prenatal diagnosis.

Prenatal diagnosis of partial trisomy 3p(3p23→pter) and monosomy 7q(7q36→qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia

K. Devriendt, Chih-ping Chen, Wayseen Wang, 1999, Prenatal diagnosis.

Prenatal diagnosis of the distal 11q deletion and review of the literature

Chih-ping Chen, C. Tzen, S. Chern, 2004, Prenatal diagnosis.

Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities.

Chih-ping Chen, T. Ko, S. Chern, 2018, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of concomitant Wolf–Hirschhorn syndrome and split hand‐foot malformation associated with partial monosomy 4p (4p16.1→pter) and partial trisomy 10q (10q25.1→qter)

Chih-ping Chen, F. Tsai, S. Chern, 2008, Prenatal diagnosis.

Array comparative genomic hybridization characterization of a 3.3-Mb 17p13.3-p13.2 deletion encompassing YWHAE, CRK, HIC1 and PAFAH1B1 in an 8-year-old girl with Miller-Dieker lissencephaly syndrome, congenital heart defects, growth restriction and developmental delay.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2018, Taiwanese journal of obstetrics & gynecology.

Rapid diagnosis of trisomy 13 of maternal origin by quantitative fluorescent polymerase chain reaction analysis in a pregnancy with fetal holoprosencephaly, premaxillary agenesis, postaxial polydactyly of left hand and overriding aorta.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2021, Taiwanese journal of obstetrics & gynecology.

Rapid Diagnosis of Trisomy 21 by Array Comparative Genomic Hybridization using Uncultured Amniocytes in a Pregnancy with Isolated Ventriculomegaly in the Fetus

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2012 .

Rapid Diagnosis of Trisomy 18 Using Uncultured Amniocytes in Late Second Trimester in a Pregnancy with Fetal Congenital Heart Defects, Arthrogryposis, Omphalocele, and Mega Cisterna Magna

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2012 .

Rapid Diagnosis of Monosomy X using Uncultured Amniocytes in Amniotic Fluid and Cultured Lymphocytes in Cystic Fluid in a Pregnancy with Fetal Cystic Hygroma and Hydrops

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2012 .

Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb.

Chih-ping Chen, S. Chern, C. Pan, 2011, Taiwanese journal of obstetrics & gynecology.

Fetal DNA in maternal plasma: the prenatal detection of a paternally inherited fetal aneuploidy

Chih-ping Chen, S. Chern, Wayseen Wang, 2000 .

Prenatal diagnosis of pentalogy of Cantrell associated with hypoplasia of the right upper limb and ectrodactyly

Chih-ping Chen, C. Tzen, S. Chern, 2007, Prenatal diagnosis.

22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae, and congenital heart defects on prenatal ultrasound.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester.

Chih-ping Chen, F. Tsai, S. Weng, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and genetic analysis of X chromosome polysomy 49,XXXXY

Chih-Long Chang, Chih-ping Chen, S. Chern, 2000, Prenatal diagnosis.

Prenatal diagnosis of microvillus inclusion disease.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18

Chih-ping Chen, S. Chern, Wayseen Wang, 2000, Prenatal diagnosis.

Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy.

Chih-ping Chen, S. Chern, Wayseen Wang, 2008, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry.

Chih-ping Chen, H. Su, S. Chern, 2013, Taiwanese journal of obstetrics & gynecology.

Concordant myelomeningocele in dizygotic twins conceived by intracytoplasmic sperm injection, in vitro fertilization, and embryo transfer.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction analysis following tissue culture failure for conventional cytogenetic analysis in a fetus with holoprosencephaly, ventricular septal defect, arthrogryposis of bilateral wrists and aplasia of the t

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2021, Taiwanese journal of obstetrics & gynecology.

Tetrasomy of 11q13.4-q14.3 due to an intrachromosomal triplication associated with paternal uniparental isodisomy for 11q14.3-qter, intrauterine growth restriction, developmental delay, corpus callosum dysgenesis, microcephaly, congenital heart defects and facial dysmorphism.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2021, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene.

Chih-ping Chen, Wayseen Wang, Yidi Su, 2011, Taiwanese journal of obstetrics & gynecology.

A 17-year-old boy with Klinefelter syndrome presenting Marfan syndrome-like clinical features of tall stature, scoliosis, arachnodactyly and subluxation of bilateral elbow joints.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2018, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result.

Chih-ping Chen, T. Ko, S. Chern, 2021, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

High-level mosaic trisomy 14 at amniocentesis in a pregnancy associated with congenital heart defects and intrauterine growth restriction on fetal ultrasound.

Chih-ping Chen, Wayseen Wang, Liang-Kai Wang, 2023, Taiwanese journal of obstetrics & gynecology.

A de novo 7.9 Mb deletion in 22q13.2→qter in a boy with autistic features, epilepsy, developmental delay, atopic dermatitis and abnormal immunological findings.

Chih-ping Chen, F. Tsai, S. Chern, 2010, European journal of medical genetics.

Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis

Chih-ping Chen, F. Tsai, S. Chern, 2003, Prenatal diagnosis.

Postnatal identi fi cation of high plasma renin activity or hypercalcemia might aid in the diagnosis

Chih-ping Chen, Wayseen Wang, Wen‐Lin Chen, 2004 .

Prenatal diagnosis of partial trisomy 3p (3p21-->pter) and partial monosomy 11q (11q23-->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2008, Journal of the Formosan Medical Association = Taiwan yi zhi.

Prenatal diagnosis of partial trisomy 3p(3p23→pter) and monosomy 7q(7q36→qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia

K. Devriendt, Chih-ping Chen, Wayseen Wang, 1999, Prenatal diagnosis.

Concomitant exencephaly and limb defects associated with pentalogy of Cantrell.

Chih-ping Chen, C. Tzen, F. Tsai, 2008, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→ter→qter)

Chih-ping Chen, Wayseen Wang, Tung-Yao Chang, 2006, Prenatal diagnosis.

Hypospadias in sons of women exposed to diethylstilbestrol in utero

C. Tzen, Wayseen Wang, Yi-Hui Lin, 2005, Prenatal diagnosis.

Hypospadias in sons of women exposed to ditheylstilbestrol: a true trans‐generational effect?

Chih-ping Chen, S. Chern, Wayseen Wang, 2005, Prenatal diagnosis.

Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1→qter)

Chih-ping Chen, C. Tzen, Wayseen Wang, 2005, Prenatal diagnosis.

Second‐trimester sonographic demonstration of retrognathia and bilateral pyelectasis in a fetus with a duplication of chromosome 10q24.1→qter

Chih-ping Chen, C. Tzen, Wayseen Wang, 2003, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Prenatal diagnosis of partial trisomy 10q (10q25.3→qter) and partial monosomy 18q (18q23→qter)

Chih-ping Chen, S. Chern, Wayseen Wang, 2005, Prenatal Diagnosis.

the cultured amniocytes showed a triallelic pattern with a dosage ratio of 1 : 0 . 12 : 1 ( paternal allele : weak heterozygous maternal allele : maternal allele )

Chih-ping Chen, S. Chern, Wayseen Wang, 2005 .

Prenatal diagnosis of concomitant gallbladder hydrops and pyelectasis with spontaneous resolution.

Chih-ping Chen, Wayseen Wang, S. Chien, 2007, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular genetic analysis of recurrent trisomy 18 of maternal origin in two consecutive pregnancies.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2023, Taiwanese journal of obstetrics & gynecology.

Prenatal three‐dimensional/four‐dimensional sonographic demonstration of facial dysmorphisms associated with holoprosencephaly

Wayseen Wang, Chin-Yuan Hsu, Chen-Yu Chen, 2005, Journal of Clinical Ultrasound.

of partial trisomy

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2022 .

Prenatal diagnosis of de novo partial trisomy 13q (13q22 → qter) and partial monosomy 8p (8p23.3 → pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart

Chih-ping Chen, S. Chern, Wayseen Wang, 2005, Prenatal diagnosis.

Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21.

Chih-ping Chen, F. Tsai, T. Ko, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome.

Chih-ping Chen, Chia-Hao Chan, S. Chern, 2021, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter).

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a positive NIPT result suspicious of trisomy 13, a CVS result of mosaic trisomy 13, cytogenetic discrepancy in various tissues and a favorable fetal outcome.

Chih-ping Chen, S. Chern, C. Pan, 2023, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes.

Chih-ping Chen, T. Ko, S. Chern, 2021, Taiwanese journal of obstetrics & gynecology.

Spontaneous resolution of septated cystic hygroma with a severely increased nuchal translucency thickness of 5.8 mm detected in the first-trimester in a pregnancy with no abnormalities in chromosomal, microarray and whole exome sequencing analyses and a favorable fetal outcome.

Chih-ping Chen, Shin-Wen Chen, Wayseen Wang, 2022, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of an acardiac amorphous twin and the anomalous co‐twin in a monoamniotic twin pregnancy

Chih-ping Chen, C. Tzen, S. Chern, 2005, Prenatal Diagnosis.

Detection of a novel c.7106_7110delinsT heterozygous mutation in the FLNA gene in an asymptomatic mother with periventricular nodular heterotopia during prenatal genetic counseling.

Chih-ping Chen, N. Chiu, S. Chern, 2016, Taiwanese Journal of Obstetrics & Gynecology.

Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of del(X)(p22.33)mat and de novo dup(4)(q34.3q35.2) in a male fetus with multiple anomalies of facial dysmorphism, ventriculomegaly, congenital heart defects, short long bones and clinodactyly.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2023, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of a familial normal euchromatic variant of dup(15)(q11.2q11.2) in a pregnancy with a favorable outcome.

Chih-ping Chen, Jian-Pei Huang, T. Ko, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of complete trisomy 16q in two consecutive pregnancies

Chih-ping Chen, Wayseen Wang, Chen‐Chi Lee, 2004, Prenatal diagnosis.

Concomitance of 47,XXY, a balanced reciprocal translocation of t(4;17)(q12;q11.2) encompassing SPINK2 at 4q12 and NOS at 17q11.2 and an AZFa sY86 deletion in an infertile male.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2023, Taiwanese journal of obstetrics & gynecology.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of monosomy 17p (17p13.3-->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly, and Miller-Dieker lissencephaly syndrome in a fetus.

Chih-ping Chen, P. Su, Wayseen Wang, 2009, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene.

Fuu-Jen Tsai, Chih-ping Chen, F. Tsai, 2010, Taiwanese journal of obstetrics & gynecology.

Androgen receptor gene mutations in 46,XY females with germ cell tumours.

Chih-ping Chen, S. Chern, Wayseen Wang, 1999, Human reproduction.

Incidental detection of familial 8p23.2 microduplication encompassing CSMD1 associated with mosaic 46,XY,t(7;8)(q31.2;p23.1)/46,XY at amniocentesis in a pregnancy with no apparent phenotypic abnormality and a favorable outcome

Chih-ping Chen, Yeou-Lih Wang, Peih-Shan Wu, 2024, Taiwanese Journal of Obstetrics and Gynecology.

Prenatal diagnosis of familial 2p15 microduplication associated with pulmonary artery stenosis, single umbilical artery and left foot postaxial polydactyly on fetal ultrasound.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2021, Taiwanese journal of obstetrics & gynecology.

Mosaic tetrasomy 9p at amniocentesis in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the aneuploid cell line and cytogenetic discrepancy in various tissues.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2023, Taiwanese journal of obstetrics & gynecology.

Identification of a deletion mutation in the short flanking repeat region of exon 44 of the COL1A1 gene in a fetus with osteogenesis imperfecta type II.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Detection of a homozygous D645E mutation of the acid α‐glucosidase gene and glycogen deposition in tissues in a second‐trimester fetus with infantile glycogen storage disease type II

Chih-ping Chen, W. Hwu, C. Tzen, 2004 .

Prenatal diagnosis of inherited satellited non‐acrocentric chromosomes

K. Devriendt, Chih-ping Chen, S. Chern, 2000, Prenatal diagnosis.

Prenatal diagnosis and perinatal findings of 17q12 microdeletion encompassing HNF1B in a fetus with bilateral hyperechogenic kidneys on fetal ultrasound and mild renal abnormality after birth, and a review of the literature of prenatal diagnosis of 17q12 microdeletion.

Chih-ping Chen, Peih-Shan Wu, Wayseen Wang, 2024, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of cystic bladder distension secondary to obstructive uropathy

Chih-ping Chen, C. Tzen, Wayseen Wang, 2000, Prenatal diagnosis.