Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma, and intrauterine growth restriction

by Chih-Ping Chen, Chin-Yuan Hsu, Yi-Ning Su, Tao-Yeuan Wang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Published 2013-03-01

Osteogenesis imperfecta type IV: Prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome

by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Ming-Huei Lin, Jun-Wei Su, Wayseen Wang
Published 2012-06-01

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 i...

by Chih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, Yi-Ning Su, Yi-Yung Chen, Jun-Wei Su, Wayseen Wang
Published 2012-06-01

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

by Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Chen-Yu Chen, Jun-Wei Su, Wayseen Wang
Published 2013-06-01

Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation

by Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Yu-Ting Chen, Chen-Chi Lee, Wayseen Wang
Published 2012-09-01

Uncomplicated vaginal delivery in two consecutive pregnancies carried to term in a woman with osteogenesis imperfecta type I and bisphosphonate treatment before conception

by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Jian-Pei Huang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Published 2012-06-01

Mosaic trisomy 14 at amniocentesis: Prenatal diagnosis and literature review

by Chih-Ping Chen, Kuo-Gon Wang, Tsang-Ming Ko, Schu-Rern Chern, Jun-Wei Su, Dai-Dyi Town, Wayseen Wang
Published 2013-09-01

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

by Chih-Ping Chen, Jin-Chung Shih, Ming-Chao Huang, Yu-Peng Liu, Jun-Wei Su, Schu-Rern Chern, Wayseen Wang
Published 2012-03-01

Pure partial monosomy 3p (3p25.3 → pter): Prenatal diagnosis and array comparative genomic hybridization characterization

by Chih-Ping Chen, Yi-Ning Su, Chen-Yu Chen, Jun-Wei Su, Schu-Rern Chern, Dai-Dyi Town, Wayseen Wang
Published 2012-09-01

Maternal transmission of interstitial microdeletion in 5q13.2 detected during prenatal diagnosis of coarctation of the aorta

by Chih-Ping Chen, Chen-Ju Lin, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wayseen Wang
Published 2013-06-01

Mosaic trisomy 12 at amniocentesis: Prenatal diagnosis and molecular genetic analysis

by Chih-Ping Chen, Yi-Ning Su, Jun-Wei Su, Schu-Rern Chern, Yu-Ting Chen, Li-Feng Chen, Wayseen Wang
Published 2013-03-01

Prenatal diagnosis of trisomy 8 mosaicism

by Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Yu-Ting Chen, Jun-Wei Su, Chen-Wen Pan, Wayseen Wang
Published 2012-12-01

Osteogenesis imperfecta type I: Second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the paucisymptomatic father

by Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Chen-Yu Chen, Jun-Wei Su, Wayseen Wang
Published 2012-06-01

Prenatal diagnosis of an interstitial deletion of 10q (10q11.21 → q21.1): Array comparative genomic hybridization characterization and literature review

by Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Dai-Dyi Town, Wayseen Wang
Published 2012-12-01

Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridizatio...

by Chih-Ping Chen, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wen-Lin Chen, Wayseen Wang
Published 2013-06-01

Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification using uncultured amniocytes in pregnancy with major fetal structural abnormalities

by Chih-Ping Chen, Yi-Ning Su, Chih-Long Chang, Yi-Yung Chen, Jun-Wei Su, Schu-Rern Chern, Wayseen Wang
Published 2012-03-01

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...

by Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen-Chi Lee, Wayseen Wang
Published 2014-03-01

Association Between Preeclampsia Risk and Fine Air Pollutants and Acidic Gases: A Cohort Analysis in Taiwan

by Shih-Yi Lin, Shih-Yi Lin, Yu-Cih Yang, Yu-Cih Yang, Jun-Wei Su, Jun-Wei Su, Jie-Sian Wang, Jie-Sian Wang, Chang-Cheng Jiang, Chang-Cheng Jiang, Chung-Y. Hsu, Chia-Hung Kao, Chia-Hung Kao, Chia-Hung Kao, Chia-Hung Kao
Published 2021-03-01

Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21)

by Chih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, Jun-Wei Su, Yu-Ting Chen, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang
Published 2013-03-01

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...

by Chih-Ping Chen, Chung-Hu Fu, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen-Chi Lee, Meng-Shan Lee, Wayseen Wang
Published 2013-09-01