Jun-Wei Su

发表

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.

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.

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.

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 .

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 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 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 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.

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.

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.

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.

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.

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 .

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.

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.

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.

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.

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.

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.

Prenatal Diagnosis of LimbeBody Wall Complex With Craniofacial Defects

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

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 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.

Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, 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.

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.

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

Chih-ping Chen, T. Ko, S. Chern, 2013, 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.

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 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.

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.

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.

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.

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.

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.

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.

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.

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.

Prenatal diagnosis of mosaic tetrasomy 18p.

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

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 .

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.

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 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.

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.

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.

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.

Conjoined twins detected in the first trimester: a review.

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

Incidental Detection of Thoracoomphalopagus at Amniocentesis in a Twin Pregnancy

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

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 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.

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.

Research Letter Prenatal diagnosis of mosaic trisomy 9

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

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 .

Cervical pregnancy: a case report of hysteroscopic resection and balloon compression combined with systematic methotrexate treatment.

Jun-Wei Su, Chih-Yi Yang, Chien-Chu Huang, 2022, 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.

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.

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.

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