Jun-Wei Su

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, Yi‐Yung Chen, Schu‐Rern Chern et al. · Taiwanese Journal of Obstetrics and Gynecology · 2013 · 56 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry

Chih‐Ping Chen, Yi‐Ning Su, Shuan‐Pei Lin et al. · Taiwanese Journal of Obstetrics and Gynecology · 2013 · 40 citations · Full text

Life Sciences, Genetics, Obstetrics +17

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, Shuenn‐Dyh Chang, Tzu‐Hao Wang et al. · Taiwanese Journal of Obstetrics and Gynecology · 2013 · 28 citations · Full text

Medicine, Genetics, Obstetrics +17

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, Yi‐Yung Chen et al. · Gene · 2013 · 21 citations

Medicine, Developmental Biology, Obstetrics +11

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, Tsang‐Ming Ko, Yi‐Yung Chen et al. · Gene · 2013 · 21 citations

Life Sciences, Genetics, Molecular Genetics +16