Third-trimester 3D Ultrasound Evaluation of Thanatophoric Dysplasia Type I

Por Chih-Ping Chen, Tung-Yao Chang, Schu-Rern Chern, Wayseen Wang
Publicado em 2007-09-01

Prenatal Magnetic Resonance Imaging Evaluation of a Digynic Triploid Fetus

Por Chih-Ping Chen, Tung-Yao Chang, Yu-Peng Liu, Schu-Rern Chern, Wayseen Wang
Publicado em 2007-09-01

Prenatal diagnosis of microvillus inclusion disease

Por Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Pei-Chen Wu, Wayseen Wang
Publicado em 2011-09-01

Concomitant Omphalocele and Anencephaly Associated with Trisomy 18 and Arthrogryposis Diagnosed in Early Pregnancy

Por Chih-Ping Chen, Tung-Yao Chang, Hung-Hung Lin, Schu-Rern Chern, Wayseen Wang
Publicado em 2008-03-01

First-trimester prenatal diagnosis of Ellis–van Creveld syndrome

Por Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Publicado em 2012-12-01

The significance of karyotyping and azoospermia factor analysis in patients with nonobstructive azoospermia or oligozoospermia

Por Shin-Wen Chen, Chih-Ping Chen, Schu-Rern Chern, Yu-Ling Kuo, Chien-Ling Chiu
Publicado em 2022-09-01

Prenatal Diagnosis and Molecular Analysis of Triploidy in a Fetus With Intrauterine Growth Restriction, Relative Macrocephaly and Holoprosencephaly

Por Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Chin-Yuan Hsu, Kevin Ko, Wayseen Wang
Publicado em 2009-09-01

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

Por Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Publicado em 2013-03-01

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

Por Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Publicado em 2012-06-01

First-trimester sonographic demonstration of digynic triploidy

Por Chih-Ping Chen, Yi-Yung Chen, Schu-Rern Chern, Yu-Ling Kuo, Chen-Chi Lee, Wayseen Wang
Publicado em 2013-12-01

Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum

Por Chih-Ping Chen, Chin-Yuan Hsu, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Wayseen Wang
Publicado em 2020-01-01

Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straigh...

Por Chih-Ping Chen, Tung-Yao Chang, Ming-Huei Lin, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Publicado em 2013-09-01

Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis

Por Chih-Ping Chen, Hsu-Kuang Huang, Yu-Peng Liu, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Publicado em 2013-12-01

Prenatal Diagnosis and Molecular Analysis of Trisomy 13 Mosaicism

Por Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Hung-Hung Lin, Chen-Wen Pan, Wayseen Wang
Publicado em 2009-09-01

Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autis...

Por Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang
Publicado em 2021-03-01

Trisomy 13 Mosaicism Associated With Cyclopia and Cystic Hygroma

Por Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Wayseen Wang
Publicado em 2009-12-01

First-trimester sonographic demonstration of digynic triploidy

Por Chih-Ping Chen, Yi-Yung Chen, Schu-Rern Chern, Yu-Ling Kuo, Chen-Chi Lee, Wayseen Wang
Publicado em 2013-12-01

Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis

Por Chih-Ping Chen, Hsu-Kuang Huang, Yu-Peng Liu, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Publicado em 2013-12-01

Discordant anencephaly and Cantrell syndrome in monozygotic twins conceived by ICSI and IVF–ET

Por Chih-Ping Chen, Ming-Chao Huang, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wayseen Wang
Publicado em 2013-06-01

Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straigh...

Por Chih-Ping Chen, Tung-Yao Chang, Ming-Huei Lin, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Publicado em 2013-09-01