Meng‐Shan Lee

发表

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.

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

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

Prenatal diagnosis 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.

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

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

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

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

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

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

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 of low‐level mosaic tetrasomy 9p by amniocentesis

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

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

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

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

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

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 .

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Unbalanced reciprocal translocations at amniocentesis.

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

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

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

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

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

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.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Chromosomal deletions detected at amniocentesis.

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

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

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

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.

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

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

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

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

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

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

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

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

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.

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

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

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 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 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 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 .

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

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

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 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 15 in a pregnancy associated with recurrent Down syndrome.

Chih-ping Chen, Chia-Hao Chan, S. Chern, 2021, 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.

Prenatal diagnosis of a familial normal euchromatic variant of dup(15)(q11.2q11.2) in a pregnancy with a favorable outcome.

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