S. Lai

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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.

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

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

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

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

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

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

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

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

Reply to Comment on An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus

Chih-ping Chen, Shin-Wen Chen, Chen‐Ju Lin, 2018, Journal of medical ultrasound.

An Intrauterine Gestational sac Surrounded by Thin Myometrium at Fundus

Chih-ping Chen, Shin-Wen Chen, Chen‐Ju Lin, 2017, Journal of medical ultrasound.

An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus

Chih-ping Chen, Shin-Wen Chen, Chen‐Ju Lin, 2017, Journal of medical ultrasound.

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

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

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

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

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

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

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

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

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

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

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

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

Pregnancies with positive non-invasive prenatal testing result for sex chromosome abnormalities in a tertiary hospital in Hong Kong

I. F. Lo, A. Kan, H. Luk, 2022, Hong Kong Journal of Gynaecology, Obstetrics and Midwifery.

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

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

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

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

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.

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

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

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

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

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.

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

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

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

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

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

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

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

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

Reply to Comment on An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus

Chih-ping Chen, Shin-Wen Chen, Chen‐Ju Lin, 2018, Journal of medical ultrasound.