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Schu-Rern Chern

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Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Chen-Ju Lin; Jun-Wei Su; Tung-Yao Chang; Peih-Shan Wu; Wayseen Wang
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.
Chih-Ping Chen; Schu-Rern Chern; Chin-Yuan Hsu; Jun-Wei Su; Yi-Ning Su; Tao-Yeuan Wang; Wayseen Wang
Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma, and intrauterine growth restriction.
Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome.

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2013: Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Chen-Ju Lin; Jun-Wei Su; Tung-Yao Chang; Peih-Shan Wu; Wayseen Wang
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.
Gene 2013;519(1):164-8.
2013: Chih-Ping Chen; Schu-Rern Chern; Chin-Yuan Hsu; Jun-Wei Su; Yi-Ning Su; Tao-Yeuan Wang; Wayseen Wang
Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma, and intrauterine growth restriction.
Taiwanese journal of obstetrics & gynecology 2013;52(1):154-6.
2013: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome.
Taiwanese journal of obstetrics & gynecology 2013;52(1):152-3.
2013: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Ho-Yen Chueh; Meng-Shan Lee; Jun-Wei Su; Yi-Ning Su; Shuenn-Dyh Chang; Wayseen Wang
Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20.
Taiwanese journal of obstetrics & gynecology 2013;52(1):145-6.
2013: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Kwui-Shuai Hwang; Shuan-Pei Lin; Her-Young Su; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry.
Taiwanese journal of obstetrics & gynecology 2013;52(1):125-8.
2013: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Meng-Shan Lee; Shuan-Pei Lin; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry.
Taiwanese journal of obstetrics & gynecology 2013;52(1):120-4.
2013: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism.
Taiwanese journal of obstetrics & gynecology 2013;52(1):106-9.
2013: Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
Taiwanese journal of obstetrics & gynecology 2013;52(1):97-105.
2013: Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Yi-Yung Chen; Schu-Rern Chern; Jun-Wei Su; Peih-Shan Wu; Wayseen Wang
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.
Gene 2013;516(1):138-42.
2013: Chih-Ping Chen; Li-Feng Chen; Wen-Lin Chen; Schu-Rern Chern; Jun-Wei Su; Yao-Lung Chang; Peih-Shan Wu; Wayseen Wang
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.
Gene 2013;516(1):132-7.
2013: Chih-Ping Chen; Yi-Wen Chen; Schu-Rern Chern; Hsiu-Chuan Chou; Tzu-Chia Lai; Ji-Min Li; Sheng-Hsiang Li; Szu-Ting Lin; Ying-Chieh Lu; Chieh-Lin Wu; Hong-Lin Chan
Proteome differences between male and female fetal cells in amniotic fluid.
Omics : a journal of integrative biology 2013;17(1):16-26.
2012: Chih-Ping Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Peih-Shan Wu; Wayseen Wang
Prenatal diagnosis of an interstitial deletion of 10q (10q11.21 → q21.1): array comparative genomic hybridization characterization and literature review.
Taiwanese journal of obstetrics & gynecology 2012;51(4):672-6.
2012: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Wen Pan; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of trisomy 8 mosaicism.
Taiwanese journal of obstetrics & gynecology 2012;51(4):666-8.
2012: Chih-Ping Chen; Chen-Yu Chen; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang
First-trimester prenatal diagnosis of Ellis-van Creveld syndrome.
Taiwanese journal of obstetrics & gynecology 2012;51(4):643-8.
2012: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Jun-Wei Su; Tsung-Hsien Su; Wayseen Wang
Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother.
Taiwanese journal of obstetrics & gynecology 2012;51(4):630-4.
2012: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Tsang-Ming Ko; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Wayseen Wang
Prenatal diagnosis of mosaic tetrasomy 18p.
Taiwanese journal of obstetrics & gynecology 2012;51(4):625-9.
2012: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Wen Pan; Jun-Wei Su; Yi-Ning Su; Peih-Shan Wu; Wayseen Wang
Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
Taiwanese journal of obstetrics & gynecology 2012;51(4):603-11.
2012: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Yu-Peng Liu; Shu-Hang Ng; Jun-Wei Su; Shuenn-Dyh Chang; Peih-Shan Wu; Wayseen Wang
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.
European journal of medical genetics 2012;55(11):666-9.
2012: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation.
Taiwanese journal of obstetrics & gynecology 2012;51(3):485-8.
2012: Chih-Ping Chen; Chen-Yu Chen; Wen-Lin Chen; Schu-Rern Chern; Yu-Peng Liu; Yi-Ning Su; Fuu-Jen Tsai; Shun-Long Weng; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(3):481-4.
2012: Chih-Ping Chen; Li-Feng Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Ho-Yen Chueh; Chen-Chi Lee; Meng-Shan Lee; Chen-Wen Pan; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Shuenn-Dyh Chang; Wayseen Wang
Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes.
Taiwanese journal of obstetrics & gynecology 2012;51(3):475-80.
2012: Chih-Ping Chen; Yu-Ting Chen; Yi-Yung Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(3):471-4.
2012: Chih-Ping Chen; Chen-Yu Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Wayseen Wang
Pure partial monosomy 3p (3p25.3 → pter): prenatal diagnosis and array comparative genomic hybridization characterization.
Taiwanese journal of obstetrics & gynecology 2012;51(3):435-9.
2012: Chih-Ping Chen; Wen-Lin Chen; Yi-Yung Chen; Schu-Rern Chern; Dai-Dyi Town; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(3):430-4.
2012: Chih-Ping Chen; Li-Feng Chen; Ming Chen; Yu-Ting Chen; Schu-Rern Chern; Alex Hwa-Jiun Hsieh; Alan Hwa-Ruey Hsieh; Dong-Jay Lee; Jun-Wei Su; Shun-Ping Chang; Peih-Shan Wu; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
Taiwanese journal of obstetrics & gynecology 2012;51(3):411-7.
2012: Chih-Ping Chen; Ming Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Meng-Shan Lee; Chen-Wen Pan; Jun-Wei Su; Yi-Ning Su; Shuenn-Dyh Chang; Wayseen Wang
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 pyelectasis.
Taiwanese journal of obstetrics & gynecology 2012;51(3):405-10.
2012: Chih-Ping Chen; You-Hsuan Chen; Schu-Rern Chern; Hsiu-Chuan Chou; Sheng-Hsiang Li; Yi-Wen Lo; Ping-Chiang Lyu; Te-Lung Tsai; Shing-Jyh Chang; Hong-Lin Chan
Placenta proteome analysis from Down syndrome pregnancies for biomarker discovery.
Molecular bioSystems 2012;8(9):2360-72.
2012: Chih-Ping Chen; Schu-Rern Chern; Ming-Chao Huang; Chun-Heng Pan; Jun-Wei Su; Yi-Ning Su; Tung-Yao Chang; Wayseen Wang
Osteogenesis imperfecta type II: prenatal diagnosis and association with increased nuchal translucency and hypoechogenicity of the cranium.
Taiwanese journal of obstetrics & gynecology 2012;51(2):315-8.
2012: Chih-Ping Chen; Schu-Rern Chern; Fang-Yu Hung; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II.
Taiwanese journal of obstetrics & gynecology 2012;51(2):312-4.
2012: Chih-Ping Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Tung-Yao Chang; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(2):308-11.
2012: Chih-Ping Chen; Schu-Rern Chern; Jian-Pei Huang; Shuan-Pei Lin; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Uncomplicated vaginal delivery in two consecutive pregnancies carried to term in a woman with osteogenesis imperfecta type I and bisphosphonate treatment before conception.
Taiwanese journal of obstetrics & gynecology 2012;51(2):305-7.
2012: Chih-Ping Chen; Chen-Yu Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Tung-Yao Chang; Wayseen Wang
Osteogenesis imperfecta type I: second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the paucisymptomatic father.
Taiwanese journal of obstetrics & gynecology 2012;51(2):276-9.
2012: Chih-Ping Chen; Schu-Rern Chern; Ming-Huei Lin; Shuan-Pei Lin; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome.
Taiwanese journal of obstetrics & gynecology 2012;51(2):271-5.
2012: Chih-Ping Chen; Yi-Yung Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Tung-Yao Chang; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(2):266-70.
2012: Chih-Ping Chen; Ming Chen; Yu-Ting Chen; Schu-Rern Chern; Jian-Pei Huang; Chen-Chi Lee; Gwo-Chin Ma; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Shun-Ping Chang; Wayseen Wang
Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
Taiwanese journal of obstetrics & gynecology 2012;51(2):245-52.
2012: Chih-Ping Chen; Schu-Rern Chern; Ming-Chao Huang; Yu-Peng Liu; Jin-Chung Shih; Jun-Wei Su; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(1):139-42.
2012: Chih-Ping Chen; Yi-Yung Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Chih-Long Chang; Wayseen Wang
Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification using uncultured amniocytes in pregnancy with major fetal structural abnormalities.
Taiwanese journal of obstetrics & gynecology 2012;51(1):123-8.
2012: Chih-Ping Chen; Chen-Yu Chen; Schu-Rern Chern; Fuu-Jen Tsai; Tao-Yeuan Wang; Tung-Yao Chang; Pei-Chen Wu; Wayseen Wang
Short rib-polydactyly syndrome type II (Majewski): prenatal diagnosis, perinatal imaging findings and molecular analysis of the NEK1 gene.
Taiwanese journal of obstetrics & gynecology 2012;51(1):100-5.
2012: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Hsu-Kuang Huang; Chen-Chi Lee; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Wayseen Wang
Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism.
Taiwanese journal of obstetrics & gynecology 2012;51(1):77-82.
2012: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Szu-Yuan Chou; Yi-Hui Lin; Yi-Ning Su; Dai-Dyi Town; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(1):71-6.
2012: C-P Chen; W-L Chen; Schu-Rern Chern; Y-L Huang; C-C Lee; Shuan-Pei Lin; J-W Su; Wayseen Wang
De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delay.
Genetic counseling (Geneva, Switzerland) 2012;23(4):497-503.
2012: C-P Chen; Schu-Rern Chern; C-C Lee; Shuan-Pei Lin; J-W Su; Y-N Su; Wayseen Wang
Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delay.
Genetic counseling (Geneva, Switzerland) 2012;23(4):447-55.
2012: C P Chen; M R Chen; Schu-Rern Chern; Meng-Shan Lee; Shuan-Pei Lin; Y P Liu; J W Su; Y N Su; Wayseen Wang
Partial monosomy 3p (3p26.2 --> pter) and partial trisomy 5q (5q34 --> qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay.
Genetic counseling (Geneva, Switzerland) 2012;23(3):405-13.
2012: C P Chen; Schu-Rern Chern; Shuan-Pei Lin; J W Su; Y N Suo; Wayseen Wang
Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type III.
Genetic counseling (Geneva, Switzerland) 2012;23(3):359-65.
2012: Chih-Ping Chen; Yann-Jang Chen; Schu-Rern Chern; C-H Hsu; Shuan-Pei Lin; Chen-Wen Pan; J-W Su; Wayseen Wang
Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocation.
Genetic counseling (Geneva, Switzerland) 2012;23(2):223-9.
2012: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; J-W Su; Y-N Su; Dai-Dyi Town; Wayseen Wang
Pure distal 9p deletion in a female infant with cerebral palsy.
Genetic counseling (Geneva, Switzerland) 2012;23(2):215-21.
2012: Chih-Ping Chen; M-R Chen; Yann-Jang Chen; Schu-Rern Chern; Meng-Shan Lee; Shuan-Pei Lin; J-W Su; Wayseen Wang
Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly.
Genetic counseling (Geneva, Switzerland) 2012;23(2):195-200.
2011: Chih-Ping Chen; Schu-Rern Chern; Chin-Yuan Hsu; Maw-Shuan Lee; Yu-Peng Liu; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(4):561-3.
2011: Chih-Ping Chen; Li-Feng Chen; Schu-Rern Chern; Chin-Yuan Hsu; Yu-Peng Liu; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly.
Taiwanese journal of obstetrics & gynecology 2011;50(4):554-7.
2011: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Fang-Yu Hung; Chen-Chi Lee; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of mosaic trisomy 9.
Taiwanese journal of obstetrics & gynecology 2011;50(4):549-53.
2011: Chih-Ping Chen; Li-Feng Chen; Wen-Lin Chen; Yu-Ting Chen; Yi-Yung Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(4):506-11.
2011: Chih-Ping Chen; Ming Chen; Yu-Ting Chen; Schu-Rern Chern; Hsu-Kuang Huang; Chen-Chi Lee; Pei-Ying Ling; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Taiwanese journal of obstetrics & gynecology 2011;50(4):492-8.
2011: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Chin-Yuan Hsu; Chen-Chi Lee; Yi-Ning Su; Wayseen Wang
Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
Taiwanese journal of obstetrics & gynecology 2011;50(4):485-91.
2011: Chih-Ping Chen; Chen-Yu Chen; Li-Feng Chen; Schu-Rern Chern; Chen-Wen Pan; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(4):479-84.
2011: Chi-Yuan Chen; Guan-Yu Chen; Schu-Rern Chern; Shiu-Feng Huang; Shiaw-Min Hwang; Wen-Hsin Lo; Hsiao-Hsuan Wu; Chih-Ping Chen; Yu-Chen Hu
Biosafety assessment of human mesenchymal stem cells engineered by hybrid baculovirus vectors.
Molecular pharmaceutics 2011;8(5):1505-14.
2011: Chih-Ping Chen; Schu-Rern Chern; Yi-Ning Su; Pei-Chen Wu; Wayseen Wang
Prenatal diagnosis of microvillus inclusion disease.
Taiwanese journal of obstetrics & gynecology 2011;50(3):399-400.
2011: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Meng-Shan Lee; Shin-Yu Lin; Yi-Ning Su; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(3):390-3.
2011: Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Schu-Rern Chern; Adam Hwa-Ming Hsieh; Chin-Yuan Hsu; Yi-Hui Lin; Yu-Peng Liu; Yi-Ning Su; Heng-Kien Au; Pei-Chen Wu; Wayseen Wang
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3).
Taiwanese journal of obstetrics & gynecology 2011;50(3):359-65.
2011: Chih-Ping Chen; Yu-Ting Chen; Yi-Yung Chen; Schu-Rern Chern; Chen-Chi Lee; Yu-Peng Liu; Yi-Ning Su; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(3):345-52.
2011: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Hung-Hung Lin; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(3):339-44.
2011: Chih-Ping Chen; Ming Chen; Yu-Ting Chen; Schu-Rern Chern; Yi-Ju Pan; Yi-Ning Su; Fuu-Jen Tsai; Wayseen Wang
Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review.
Taiwanese journal of obstetrics & gynecology 2011;50(3):331-8.
2011: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p.
Taiwanese journal of obstetrics & gynecology 2011;50(2):249-52.
2011: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Chi-Hsin Chiang; Chen-Chi Lee; Jui-Der Liou; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2011;50(2):245-8.
2011: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Ming-Huei Lin; Chen-Wen Pan; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.
Taiwanese journal of obstetrics & gynecology 2011;50(2):205-11.
2011: Chih-Ping Chen; Li-Feng Chen; Ming Chen; Wen-Lin Chen; Schu-Rern Chern; Chen-Wen Pan; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
Taiwanese journal of obstetrics & gynecology 2011;50(2):188-95.
2011: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Yau-Kun Kuo; Yi-Ning Su; Dai-Dyi Town; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(2):182-7.
2011: Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Chin-Yuan Hsu; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Meng-Shan Lee; Wayseen Wang
Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
Taiwanese journal of obstetrics & gynecology 2011;50(1):67-73.
2011: Chih-Ping Chen; Pei-Chen Wu; Chen-Ju Lin; Schu-Rern Chern; Fuu-Jen Tsai; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
Unbalanced reciprocal translocations at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2011;50(1):48-57.
2011: Chih-Ping Chen; Yann-Jang Chen; Schu-Rern Chern; Meng-Shan Lee; Shuan-Pei Lin; Fuu-Jen Tsai; Wayseen Wang
Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disability.
Genetic counseling (Geneva, Switzerland) 2011;22(4):425-30.
2011: Chih-Ping Chen; M Chen; Yann-Jang Chen; Schu-Rern Chern; Chen-Chi Lee; Shuan-Pei Lin; Y P Liu; Y N Su; Fuu-Jen Tsai; T Y Wang; Wayseen Wang
Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy facial asymmetry psychomotor retardation kyphoscoliosis dermatofibrosarcoma and multiple exostoses.
Genetic counseling (Geneva, Switzerland) 2011;22(3):273-80.
2011: Chih-Ping Chen; L F Chen; Schu-Rern Chern; Shuan-Pei Lin; Y N Su; Fuu-Jen Tsai; P C Wu; Wayseen Wang
A 24.2-Mb deletion of 4q12 --> q21.21 characterized by array CGH in a 131/2-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed puberty.
Genetic counseling (Geneva, Switzerland) 2011;22(3):255-61.
2011: Schu-Rern Chern; Chien-Ling Chiu; Sheng-Hsiang Li; Hsiao-Ho Chang; Chih-Ping Chen; Edmund I Tsuen Chen
Spatiotemporal expression of SERPINE2 in the human placenta and its role in extravillous trophoblast migration and invasion.
Reproductive biology and endocrinology : RB&E 2011;9():106.
2010: Chih-Ping Chen; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Chin-Yuan Hsu; Pei-Chen Wu; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
Partial trisomy 10q (10q25.1 →qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization.
Taiwanese journal of obstetrics & gynecology 2010;49(4):539-43.
2010: Chih-Ping Chen; Yi-Ning Su; Richard Shih-Hung Young; Fuu-Jen Tsai; Pei-Chen Wu; Schu-Rern Chern; Dai-Dyi Town; Chen-Wen Pan; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2010;49(4):506-12.
2010: Chih-Ping Chen; Ming-Chou Chiang; Tzu-Hao Wang; Chuen Hsueh; Shueen-Dyh Chang; Fuu-Jen Tsai; Chao-Ning Wang; Schu-Rern Chern; Wayseen Wang
Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea.
Taiwanese journal of obstetrics & gynecology 2010;49(4):487-94.
2010: Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Po-Tsang Chen; Wayseen Wang
Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling.
Taiwanese journal of obstetrics & gynecology 2010;49(4):481-6.
2010: Chih-Ping Chen; Ming Chen; Yi-Ning Su; Chin-Yuan Hsu; Fuu-Jen Tsai; Schu-Rern Chern; Pei-Chen Wu; Chen-Chi Lee; Wayseen Wang
Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Taiwanese journal of obstetrics & gynecology 2010;49(4):473-80.
2010: Chih-Ping Chen; Pei-Chen Wu; Chen-Ju Lin; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
Balanced reciprocal translocations detected at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2010;49(4):455-67.
2010: Chih-Ping Chen; Chyi-Chyang Lin; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Wen-Ling Chen; Li-Feng Chen; Pei-Chen Wu; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22.
Taiwanese journal of obstetrics & gynecology 2010;49(3):381-4.
2010: Chih-Ping Chen; Chyi-Chyang Lin; Tsang-Ming Ko; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Yu-Ting Chen; Pei-Chen Wu; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21.
Taiwanese journal of obstetrics & gynecology 2010;49(3):377-80.
2010: Chih-Ping Chen; Hsien-Ming Lin; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
Taiwanese journal of obstetrics & gynecology 2010;49(3):341-50.
2010: Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Yuh-Ming Hwu; Shuan-Pei Lin; Chyong-Hsin Hsu; Fuu-Jen Tsai; Tao-Yeuan Wang; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Li-Feng Chen; Wayseen Wang
Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
Taiwanese journal of obstetrics & gynecology 2010;49(3):333-40.
2010: Chih-Ping Chen; Ming Chen; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Chin-Yuan Hsu; Pei-Chen Wu; Dai-Dyi Town; Dong-Jay Lee; Gwo-Chin Ma; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2010;49(3):320-6.
2010: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Wen-Ling Chen; Wayseen Wang
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.
European journal of medical genetics 2010;53(5):329-32.
2010: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Yann-Jang Chen; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
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.
European journal of medical genetics 2010;53(4):217-20.
2010: Chih-Ping Chen; Schu-Rern Chern; Chia-Hsun Wu; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Detection of balanced homologous acrocentric rearrangement rea(14q14q) and low-grade X-chromosome mosaicism in a couple with repeated pregnancy losses.
Taiwanese journal of obstetrics & gynecology 2010;49(2):239-42.
2010: Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Hsiao-En Cindy Chen; Shu-Shien Chiang; Wayseen Wang
Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation.
Taiwanese journal of obstetrics & gynecology 2010;49(2):235-8.
2010: Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Chen-Yu Chen; Fuu-Jen Tsai; Yu-Peng Liu; Schu-Rern Chern; Pei-Chen Wu; Hsiao-En Cindy Chen; Wayseen Wang
Apert syndrome associated with upper airway obstruction and gastroesophageal reflux inducing polyhydramnios in the third trimester.
Taiwanese journal of obstetrics & gynecology 2010;49(2):231-4.
2010: Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Tao-Yeuan Wang; Fuu-Jen Tsai; Hung-Hung Lin; Pei-Chen Wu; Wayseen Wang
Detection and comparison of cytomegalovirus DNA levels in amniotic fluid and fetal ascites in a second-trimester fetus with massive ascites, hyperechogenic bowel, ventriculomegaly and intrauterine growth restriction.
Taiwanese journal of obstetrics & gynecology 2010;49(2):206-10.
2010: Chih-Ping Chen; Chyi-Chyang Lin; Yi-Ning Su; Fuu-Jen Tsai; Ju-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Li-Feng Chen; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2010;49(2):188-91.
2010: Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Pei-Ying Ling; Fuu-Jen Tsai; Schu-Rern Chern; Pei-Chen Wu; Hsiao-En Cindy Chen; Wayseen Wang
Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18.
Taiwanese journal of obstetrics & gynecology 2010;49(1):129-32.
2010: Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Fuu-Jen Tsai; Shu-Chin Chien; Schu-Rern Chern; Meng-Shan Lee; Pei-Chen Wu; Hsiao-En Cindy Chen; Wayseen Wang
Abnormally flat facial profile on two- and three-dimensional ultrasound and array comparative genomic hybridization for the diagnosis of Pallister-Killian syndrome.
Taiwanese journal of obstetrics & gynecology 2010;49(1):124-8.
2010: Chih-Ping Chen; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Chin-Yuan Hsu; Ming-Chao Huang; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2010;49(1):120-3.
2010: Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Chin-Yuan Hsu; Chen-Chi Lee; Wayseen Wang
Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21 --> q11.23 by array comparative genomic hybridization.
Taiwanese journal of obstetrics & gynecology 2010;49(1):117-9.
2010: Chih-Ping Chen; Schu-Rern Chern; Pei-Chen Wu; Fuu-Jen Tsai; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
Unbalanced and balanced heterologous acrocentric rearrangements involving chromosome 21 at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2010;49(1):62-8.
2010: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Fuu-Jen Tsai; Tao-Yeuan Wang; Hung-Hung Lin; Wayseen Wang
Prenatal diagnosis of X-linked myotubular myopathy.
Prenatal diagnosis 2010;30(2):177-9.
2010: Schu-Rern Chern; Sheng-Hsiang Li; Chung-Hao Lu; Edmund I Tsuen Chen
Spatiotemporal expression of the serine protease inhibitor, SERPINE2, in the mouse placenta and uterus during the estrous cycle, pregnancy, and lactation.
Reproductive biology and endocrinology : RB&E 2010;8():127.
2009: Chih-Ping Chen; Maw-Shuan Lee; Fuu-Jen Tsai; Ming-Chao Huang; Schu-Rern Chern; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2009;48(4):446-50.
2009: Chih-Ping Chen; Yi-Ning Su; Fuu-Jen Tsai; Hung-Hung Lin; Schu-Rern Chern; Meng-Shan Lee; Jonathan Kwei Hwang; Teresa Hsiao-Tien Chen; Wayseen Wang
Terminal 2q deletion and distal 15q duplication: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes.
Taiwanese journal of obstetrics & gynecology 2009;48(4):441-5.
2009: Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Schu-Rern Chern; Fuu-Jen Tsai; Jonathan Kwei Hwang; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2009;48(4):437-40.
2009: Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Wayseen Wang
Trisomy 13 mosaicism associated with cyclopia and cystic hygroma.
Taiwanese journal of obstetrics & gynecology 2009;48(4):434-6.
2009: Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Shu-Shien Chiang; Chen-Chi Lee; Wayseen Wang
Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis.
Taiwanese journal of obstetrics & gynecology 2009;48(4):403-7.
2009: Chih-Ping Chen; Schu-Rern Chern; Pei-Chen Wu; Fuu-Jen Tsai; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2009;48(4):389-99.
2009: Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Chin-Yuan Hsu; Kevin Ko; Wayseen Wang
Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly.
Taiwanese journal of obstetrics & gynecology 2009;48(3):323-6.
2009: Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Hung-Hung Lin; Chen-Wen Pan; Wayseen Wang
Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism.
Taiwanese journal of obstetrics & gynecology 2009;48(3):321-2.
2009: Chih-Ping Chen; Fuu-Jen Tsai; Schu-Rern Chern; Tung-Yao Chang; Chin-Yuan Hsu; Hung-Hung Lin; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2009;48(1):84-7.
2009: Chih-Ping Chen; Chin-Yuan Tzen; Schu-Rern Chern; Fuu-Jen Tsai; Chin-Yuan Hsu; Chen-Chi Lee; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
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.
European journal of medical genetics 2009;52(1):59-61.
2008: Ruu-Fen Tzeng; Shen-Ing Liu; Lawrence S H Wu; Shu-Ting Chen; Yen-Hsin Yu; Pei-Chuan Li; Schu-Rern Chern; Pei-Yin Lee; Tsuo-Hung Lan; El-Wui Loh
High proportion of single CYP2D6 gene deletion in Chinese attention-deficit-hyperactivity disorder children and its risk in oppositional defiant disorder.
Psychiatry and clinical neurosciences 2008;62(6):749.
2008: Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Tzu-Hao Wang; Schu-Rern Chern; Wayseen Wang
Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review.
Fertility and sterility 2008;90(4):1198.e11-8.
2008: Chih-Ping Chen; Yann-Jang Chen; Schu-Rern Chern; Fuu-Jen Tsai; Hung-Hung Lin; Chen-Chi Lee; Wayseen Wang
Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.
Prenatal diagnosis 2008;28(9):865-7.
2008: Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang
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.
European journal of medical genetics 2008;51(4):368-72.
2008: Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Schu-Rern Chern; Wayseen Wang
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation.
Fertility and sterility 2008;89(6):1826.e5-7.
2008: Chih-Ping Chen; Yann-Jang Chen; Schu-Rern Chern; Fuu-Jen Tsai; Tung-Yao Chang; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Lee; Wayseen Wang
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).
Prenatal diagnosis 2008;28(5):450-3.
2008: Chih-Ping Chen; Yann-Jang Chen; Fuu-Jen Tsai; Schu-Rern Chern; Wayseen Wang
NFkappaB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1 --> qter).
Prenatal diagnosis 2008;28(4):364-5.
2008: Chih-Ping Chen; Jin-Chung Shih; Chin-Yuan Tzen; Schu-Rern Chern; Chen-Ju Lin; Wayseen Wang
Prenatal visualization of cebocephaly with a prominent nose in a second-trimester fetus with alobar holoprosencephaly and trisomy 13.
Taiwanese journal of obstetrics & gynecology 2008;47(1):95-7.
2008: Chih-Ping Chen; Tung-Yao Chang; Hung-Hung Lin; Schu-Rern Chern; Wayseen Wang
Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy.
Taiwanese journal of obstetrics & gynecology 2008;47(1):93-4.
2007: Chih-Ping Chen; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Wayseen Wang
Cytogenetic variability in the proportion of abnormal cells between the various tissues in prenatally detected mosaic tetrasomy 12p.
Prenatal diagnosis 2007;27(12):1170-3.
2007: Chih-Ping Chen; Tzu-Hao Wang; Yann-Jang Chen; Tung-Yao Chang; Yu-Peng Liu; Chin-Yuan Tzen; Schu-Rern Chern; Wayseen Wang
Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1.
Prenatal diagnosis 2007;27(10):967-9.
2007: Chih-Ping Chen; Tung-Yao Chang; Yu-Peng Liu; Schu-Rern Chern; Wayseen Wang
Prenatal magnetic resonance imaging evaluation of a digynic triploid fetus.
Taiwanese journal of obstetrics & gynecology 2007;46(3):284-5.
2007: Chih-Ping Chen; Tung-Yao Chang; Schu-Rern Chern; Wayseen Wang
Third-trimester 3D ultrasound evaluation of thanatophoric dysplasia type I.
Taiwanese journal of obstetrics & gynecology 2007;46(3):281-3.
2007: Chih-Ping Chen; Tung-Yao Chang; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Lee; Wayseen Wang
Prenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesis.
Prenatal diagnosis 2007;27(4):383-5.
2007: Chih-Ping Chen; Chen-Ju Lin; Tung-Yao Chang; Schu-Rern Chern; Chin-Yuan Tzen; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of the hypoplastic right heart syndrome with sex chromosome pentasomy (49,XXXXY).
Prenatal diagnosis 2007;27(3):285-6.
2007: Chih-Ping Chen; S C Chien; Schu-Rern Chern; Chin-Yuan Tzen; Wayseen Wang
Prenatal diagnosis of Dandy-Walker malformation associated with distal limb deficiencies.
Genetic counseling (Geneva, Switzerland) 2007;18(3):343-7.
2007: Chien-Liang Liu; Yuan-Ching Chang; Shih-Ping Cheng; Schu-Rern Chern; Tsen-Long Yang; Jie-Jen Lee; Ing-Cherng Guo; Chih-Ping Chen
The roles of serum leptin concentration and polymorphism in leptin receptor gene at codon 109 in breast cancer.
Oncology 2007;72(1-2):75-81.
2007: Chih-Ping Chen; Shuan-Pei Lin; Chin-Yuan Tzen; W L Hwu; Schu-Rern Chern; Chih-Kuang Chuang; S S Chiang; Wayseen Wang
Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome).
Genetic counseling (Geneva, Switzerland) 2007;18(1):49-56.
2007: Chih-Ping Chen; Chin-Yuan Hsu; Chin-Yuan Tzen; Schu-Rern Chern; Wayseen Wang
Prenatal diagnosis of pentalogy of Cantrell associated with hypoplasia of the right upper limb and ectrodactyly.
Prenatal diagnosis 2007;27(1):86-7.
2006: Chih-Ping Chen; Schu-Rern Chern; Pei-Yin Lee; Dai-Dyi Town; Wayseen Wang
Prenatal diagnosis of low-level mosaic trisomy 6 by amniocentesis.
Prenatal diagnosis 2006;26(11):1093-6.
2006: Chih-Ping Chen; Tzu-Hao Wang; Shuan-Pei Lin; Schu-Rern Chern; M-R Chen; Chen-Chi Lee; Yann-Jang Chen; Wayseen Wang
24 Mb deletion of 6q22.1-->q23.2 in an infant with pulmonary atresia, ventricular septal defect, microcephaly, developmental delay and facial dysmorphism.
European journal of medical genetics 2006;49(6):516-9.
2006: Chih-Ping Chen; Tzu-Hao Wang; Schu-Rern Chern; Chin-Yuan Tzen; Chin-Yuan Hsu; Chen-Chi Lee; Li-Feng Chen; Chung-Chun Ma; Po-Tsang Chen; Wayseen Wang
Prenatal diagnosis of congenital chylothorax associated with de novopartial trisomy 12q (12q21.2-->qter).
Prenatal diagnosis 2006;26(8):752-5.
2006: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yann-Jang Chen; Schu-Rern Chern; Yueh-Chun Li; Lie-Jiau Hsieh; Chen-Chi Lee; Chen-Wen Pan; Wayseen Wang
Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q.
American journal of medical genetics. Part A 2006;140(14):1594-600.
2006: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Schu-Rern Chern; Chen-Chi Lee; Li-Feng Chen; Hui-Min Hua; Wayseen Wang
Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetus.
Prenatal diagnosis 2006;26(4):387-91.
2006: Chih-Ping Chen; Schu-Rern Chern; Chyi-Chyang Lin; Tzu-Hao Wang; Yueh-Chun Li; Lie-Jiau Hsieh; Chen-Chi Lee; Hui-Min Hua; Wayseen Wang
Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
Prenatal diagnosis 2006;26(4):313-20.
2006: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Wen-Lin Chen; Wayseen Wang
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.
Prenatal diagnosis 2006;26(2):138-46.
2006: Chih-Ping Chen; Schu-Rern Chern; Fang-Yu Hung; Chin-Yuan Hsu; Tung-Yao Chang; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Chin-Yuan Tzen; Wayseen Wang; Ryan Ma
Prenatal diagnosis of pure distal 18q deletion.
Prenatal diagnosis 2006;26(2):184-5.
2006: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Chyi-Chyang Lin; Yueh-Chun Li; Chen-Chi Lee; Lie-Jiau Hsieh; Wen-Lin Chen; Wayseen Wang
Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings.
Prenatal diagnosis 2006;26(2):181-3.
2006: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Chen-Chi Lee; Jon-Kway Huang; Wayseen Wang
Direct transmission of the 18q- syndrome from mother to daughter.
Genetic counseling (Geneva, Switzerland) 2006;17(2):185-9.
2005: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Schu-Rern Chern; Chen-Chi Lee; Yen-Jiun Chen; Wayseen Wang
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).
Prenatal diagnosis 2005;25(12):1170-2.
2005: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Tzu-Hao Wang; Chen-Chi Lee; Chen-Wen Pan; Lie-Jiau Hsieh; Wayseen Wang
A paternally derived inverted duplication of distal 14q with a terminal 14q deletion.
American journal of medical genetics. Part A 2005;139A(2):146-50.
2005: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of partial trisomy 10q (10q25.3-->qter) and partial monosomy 18q (18q23-->qter).
Prenatal diagnosis 2005;25(11):1069-71.
2005: Chih-Ping Chen; Schu-Rern Chern; Li-Feng Chen; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis.
Prenatal diagnosis 2005;25(11):1067-9.
2005: Chih-Ping Chen; Jin-Chung Shih; Tung-Yao Chang; Schu-Rern Chern; Ching-Yi Lin; Wayseen Wang; Chin-Yuan Tzen
Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy.
Prenatal diagnosis 2005;25(7):618-20.
2005: Chih-Ping Chen; Schu-Rern Chern; Jin-Chern Sheu; Shuan-Pei Lin; Chin-Yuan Hsu; Tung-Yao Chang; Chen-Chi Lee; Wayseen Wang; Hsiao-En Cindy Chen
Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera.
Prenatal diagnosis 2005;25(6):502-6.
2005: Chih-Ping Chen; Schu-Rern Chern; Tzu-Hao Wang; Ding-Wei Hsueh; Chen-Chi Lee; Dai-Dyi Town; Wayseen Wang; Tsang-Ming Ko
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.
Prenatal diagnosis 2005;25(6):492-6.
2005: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang; Hsiao-En Cindy Chen
Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency.
Prenatal diagnosis 2005;25(5):383-9.
2005: Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Ching-Yi Lin; Yi-Hui Lin; Wayseen Wang
A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error.
Prenatal diagnosis 2005;25(4):327-30.
2005: Chih-Ping Chen; Schu-Rern Chern; Chin-Yuan Hsu; Chen-Chi Lee; Meng-Shan Lee; Wayseen Wang
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.
Prenatal diagnosis 2005;25(4):334-6.
2005: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Schu-Rern Chern; Wei-Min Chen; Chen-Chi Lee; Lie-Jiau Hsieh; Wayseen Wang
Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
Prenatal diagnosis 2005;25(2):112-8.
2005: Hui-Ju Chen; Shuan-Pei Lin; Hung-Chang Lee; Chih-Ping Chen; Nan-Chang Chiu; Han-Yang Hung; Schu-Rern Chern; Chih-Kuang Chuang
Cystic fibrosis with homozygous R553X mutation in a Taiwanese child.
Journal of human genetics 2005;50(12):674-8.
2005: Chih-Ping Chen; Schu-Rern Chern; Chen-Ju Lin; Chen-Chi Lee; Wayseen Wang; Chin-Yuan Tzen
A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephaly.
Genetic counseling (Geneva, Switzerland) 2005;16(1):49-57.
2004: Chih-Ping Chen; Chyi-Chyang Lin; Yueh-Chun Li; Schu-Rern Chern; Chen-Chi Lee; Wen-Lin Chen; Men-Shan Lee; Wayseen Wang; Chin-Yuan Tzen
Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature.
Prenatal diagnosis 2004;24(10):767-73.
2004: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Shuan-Pei Lin; Tung-Yao Chang; Wayseen Wang
Prenatal diagnosis of mosaic 22q11.2 microdeletion.
Prenatal diagnosis 2004;24(8):660-2.
2004: Chih-Ping Chen; Schu-Rern Chern; Shojen Cheng; Tung-Yao Chang; Li-Fan Yeh; Chen-Chi Lee; Chen-Wen Pan; Wayseen Wang; Chin-Yuan Tzen
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.
Prenatal diagnosis 2004;24(6):455-62.
2004: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of interstitially satellited 6p.
Prenatal diagnosis 2004;24(6):430-3.
2004: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chin-Yuan Tzen; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
Prenatal diagnosis of the distal 11q deletion and review of the literature.
Prenatal diagnosis 2004;24(2):130-6.
2004: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Chen-Chi Lee; Jon-Kway Huang; Wayseen Wang; You-Wei Liao
De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
Genetic counseling (Geneva, Switzerland) 2004;15(4):437-42.
2004: Chih-Ping Chen; Jin-Chung Shih; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang
Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha-fetoprotein and human chorionic gonadotrophin.
Prenatal diagnosis 2004;24(1):63-6.
2004: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Tung-Yao Chang; Wayseen Wang; Chin-Yuan Tzen
Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
Prenatal diagnosis 2004;24(1):38-44.
2003: Chih-Ping Chen; Schu-Rern Chern; Dai-Dyi Town; Wayseen Wang; You-Wei Liao
Fetoplacental and fetoamniotic chromosomal discrepancies in prenatally detected mosaic trisomy 9.
Prenatal diagnosis 2003;23(12):1019-21.
2003: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Li-Feng Chen; Daniel T H Chin; Chin-Yuan Tzen; Wayseen Wang
Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
Prenatal diagnosis 2003;23(9):758-61.
2003: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Shin-Lin Shih; Chen-Chi Lee; Wayseen Wang; You-Wei Liao
Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
Prenatal diagnosis 2003;23(6):504-8.
2003: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chin-Yuan Tzen; Chen-Chi Lee; Wen-Lin Chen; Meng-Shan Lee; Wayseen Wang
Prenatal diagnosis of de novo terminal deletion of chromosome 7q.
Prenatal diagnosis 2003;23(5):375-9.
2003: Chih-Ping Chen; Yuh-Ming Hwu; Li-Fan Yeh; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang
Successful triplet pregnancy and delivery after oocyte donation in an infertile female with chromosome mosaicism for monosomy X, partial trisomy X, and terminal Xp deletion.
Fertility and sterility 2003;79(5):1231-3.
2003: Chih-Ping Chen; Tung-Yao Chang; Schu-Rern Chern; Dai-Dyi Town; Chen-Wen Pan; Meng-Shan Lee; Wayseen Wang
Early second-trimester diagnosis of monozygotic twins discordant for cystic hygroma colli and Turner syndrome.
Prenatal diagnosis 2003;23(4):352-3.
2003: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Wayseen Wang; Fuu-Jen Tsai
Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis.
Prenatal diagnosis 2003;23(2):175-6.
2003: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chen-Chi Lee; Li-Feng Chen; Chin-Yuan Tzen; Wayseen Wang; Chen-Ju Lin; Brian P T Yang; Lawrence S T Yang
Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.
Prenatal diagnosis 2003;23(1):40-3.
2002: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chen-Ju Lin; Wayseen Wang; Chin-Yuan Tzen
Second trimester molecular diagnosis of a stop codon FGFR3 mutation in a type I thanatophoric dysplasia fetus following abnormal ultrasound findings.
Prenatal diagnosis 2002;22(8):736-7.
2002: Chih-Ping Chen; Schu-Rern Chern; Shin-Hua Du; Wayseen Wang
Molecular diagnosis of a novel heterozygous 268C-->T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis.
Prenatal diagnosis 2002;22(1):5-7.
2001: Chih-Ping Chen; Schu-Rern Chern; Wayseen Wang; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Tung-Yao Chang; Chin-Yuan Tzen
Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Prenatal diagnosis 2001;21(5):346-50.
2001: Chih-Ping Chen; Schu-Rern Chern; Chin-Yuan Tzen; Meng-Shan Lee; Chen-Wen Pan; Tung-Yao Chang; Wayseen Wang
Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts.
Prenatal diagnosis 2001;21(4):317-20.
2001: Chih-Ping Chen; Schu-Rern Chern; Wayseen Wang; K L Wang; Tao-Yeuan Wang
Multiple globules in a cystic ovarian teratoma.
Fertility and sterility 2001;75(3):618-9.
2001: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly.
Prenatal diagnosis 2001;21(2):102-5.
2001: Chih-Ping Chen; Schu-Rern Chern; Jin-Chung Shih; Wayseen Wang; Li-Fan Yeh; Tung-Yao Chang; Chin-Yuan Tzen
Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia.
Prenatal diagnosis 2001;21(2):89-95.
2000: Chih-Ping Chen; Schu-Rern Chern; C L Chang; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
Prenatal diagnosis and genetic analysis of X chromosome polysomy 49, XXXXY.
Prenatal diagnosis 2000;20(9):754-7.
2000: Chih-Ping Chen; Schu-Rern Chern; Li-Fan Yeh; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18.
Prenatal diagnosis 2000;20(9):750-3.
2000: C P Chen; Schu-Rern Chern; Be-Fong Chen; W Wang; Y M Hwu
Hamartoma in a pubertal patient with complete androgen insensitivity syndrome and R(831)X mutation of the androgen receptor gene.
Fertility and sterility 2000;74(1):182-3.
2000: Chih-Ping Chen; koenraad devriendt; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang; Shuan-Pei Lin
Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
Prenatal diagnosis 2000;20(5):384-9.
2000: Schu-Rern Chern; Chih-Ping Chen
Molecular prenatal diagnosis of thalassemia in Taiwan.
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics 2000;69(2):103-6.
2000: Chih-Ping Chen; Schu-Rern Chern; Wayseen Wang
Rapid determination of zygosity and common aneuploidies from amniotic fluid cells using quantitative fluorescent polymerase chain reaction following genetic amniocentesis in multiple pregnancies.
Human reproduction (Oxford, England) 2000;15(4):929-34.
1999: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Wayseen Wang
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).
Prenatal diagnosis 1999;19(8):783-6.
1999: Chih-Ping Chen; Schu-Rern Chern; Tao-Yeuan Wang; Wayseen Wang; Kung-Liahng Wang; CJ Jeng
Androgen receptor gene mutations in 46,XY females with germ cell tumours.
Human reproduction (Oxford, England) 1999;14(3):664-70.
1998: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Wen-Lin Chen; M H Chen; K M Chang
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.
Journal of medical genetics 1998;35(12):1050-3.
1998: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town
Isochromosome 18q in a fetus with congenital megacystis, intra-uterine growth retardation and cloacal dysgenesis sequence.
Prenatal diagnosis 1998;18(10):1068-74.
1998: Chih-Ping Chen; Schu-Rern Chern; S P Lin; P Y Chang; K M Chang; F J Hsieh
Concomitant chyloperitoneum and omental cysts presenting as fetal ascites with intra-abdominal cysts on prenatal ultrasound.
Prenatal diagnosis 1998;18(9):984-6.
1998: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Li-Feng Chen; CY Chuang
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.
Prenatal diagnosis 1998;18(5):490-5.
1998: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Li-Feng Chen; CY Chuang; M H Chen
Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus.
Prenatal diagnosis 1998;18(4):393-8.
1998: Chih-Ping Chen; Schu-Rern Chern; CY Chuang; Be-Fong Chen
Prenatal detection of human cytomegalovirus DNA in fetal ascites by the polymerase chain reaction.
Acta obstetricia et gynecologica Scandinavica 1998;77(4):466-7.
1998: Chih-Ping Chen; Schu-Rern Chern; Shin-Lin Shih; CY Chuang; F Y Huang
Kyphomelic dysplasia in two sib fetuses.
Journal of medical genetics 1998;35(1):65-9.
1997: Chih-Ping Chen; Schu-Rern Chern; Tao-Yeuan Wang; Z D Huang; M C Huang; CY Chuang
Pregnancy with concomitant chorangioma and placental vascular malformation with mesenchymal hyperplasia.
Human reproduction (Oxford, England) 1997;12(11):2553-6.
1997: Chih-Ping Chen; Schu-Rern Chern; FF Liu; SW Jan; Chen-Chi Lee; Y C Chang; C T Yue
Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive results.
Prenatal diagnosis 1997;17(6):571-6.
1997: Chih-Ping Chen; H C Chen; FF Liu; SW Jan; Schu-Rern Chern; Tao-Yeuan Wang; Han-Yang Hung
Cutis marmorata telangiectatica congenita associated with an elevated maternal serum human chorionic gonadotrophin level and transitory isolated fetal ascites.
The British journal of dermatology 1997;136(2):267-71.
1997: Chih-Ping Chen; Schu-Rern Chern; FF Liu; SW Jan; H C Lee; Jin-Chern Sheu; W T Lee; Tao-Yeuan Wang
Prenatal diagnosis, pathology, and genetic study of fetus in fetu.
Prenatal diagnosis 1997;17(1):13-21.