Chen‐Chi Lee

发表

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.

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.

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.

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.

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.

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.

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.

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.

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.

PRENATAL DIAGNOSIS OF A DELETION OF 18q IN A FETUS ASSOCIATED WITH MULTIPLE‐MARKER SCREEN POSITIVE RESULTS

C. Yue, Chih-ping Chen, S. Chern, 1997, 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Cytogenetic evaluation of cystic hygroma associated with hydrops fetalis, oligohydramnios or intrauterine fetal death: the roles of amniocentesis, postmortem chorionic villus sampling and cystic hygroma paracentesis

Chih-ping Chen, Chen‐Chi Lee, D. Town, 1996, Acta obstetricia et gynecologica Scandinavica.

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 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.

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 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.

Isochromosome 18q in a fetus with congenital megacystis, intra‐uterine growth retardation and cloacal dysgenesis sequence

Chih-ping Chen, S. Chern, Chen‐Chi Lee, 1998, Prenatal diagnosis.

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.

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.

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 .

Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus

Chih-ping Chen, S. Chern, Ming-Hong Chen, 1998, Prenatal diagnosis.

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 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.

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.

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 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.

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.

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.

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.

Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, uinary tract anomalies, congenital heart defect and kyphoscoliosis

Chih-ping Chen, C. Pan, Chen‐Chi Lee, 1998, Prenatal diagnosis.

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.

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.

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.

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.

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 diagnosis of mosaic ring chromosome 13 with anencephaly

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

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.

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.

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 partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21) (p13.3;q21)

Chih-ping Chen, Shuan-Pei Lin, Wen‐Lin Chen, 1997, Prenatal diagnosis.

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 .

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.

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.

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 inherited satellited non‐acrocentric chromosomes

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

Prenatal diagnosis of mosaic ring chromosome 9

Chih-ping Chen, Wayseen Wang, Chen‐Chi Lee, 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.

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.

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 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.

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 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 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.

Chromosomal deletions detected at amniocentesis.

Chih-ping Chen, C. Pan, Wen‐Lin Chen, 2014, Taiwanese journal of obstetrics & gynecology.

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 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.

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.

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 of mosaic distal 5p deletion and review of the literature

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

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 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.

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.

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.

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.

Higher male prevalence of chromosomal mosaicism detected by amniocentesis.

Chih-ping Chen, Shin-Wen Chen, C. Pan, 2018, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of de novo interstitial 16q deletion in a fetus associated with sonographic findings of prominent coronal sutures, a prominent frontal bone, and shortening of the long bones

Chih-ping Chen, S. Chern, Chen‐Chi Lee, 1998, Prenatal diagnosis.

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.

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 .

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

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

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.

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 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 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 .

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 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 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.

Recurrent omphalocele with partial trisomy 3q and partial monosomy 11q

Chih-ping Chen, Ming-Hong Chen, Chen‐Chi Lee, 1997, Clinical genetics.

De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation, Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy, and partial hemihypoplasia.

Chih-ping Chen, S. Chern, Wen‐Lin Chen, 1998, Journal of medical genetics.

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.

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.

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.

Prenatal diagnosis of inherited satellited non‐acrocentric chromosomes

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