Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes
Chen, Chih-Ping, Wang, Yeou-Lih, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Yen-Ni, Chen, Shin-Wen, Chen, Li-Feng, Lee, Meng-Shan, Yang, Chien-Wen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.04.2016)
Published in Taiwanese journal of obstetrics & gynecology (01.04.2016)
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Journal Article
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
Chen, Chih-Ping, Chang, Tung-Yao, Lin, Tan-Wei, Chern, Schu-Rern, Chen, Shin-Wen, Lai, Shih-Ting, Chuang, Tzu-Yun, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.02.2018)
Published in Taiwanese journal of obstetrics & gynecology (01.02.2018)
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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
Chen, Chih-Ping, Chen, Ming, Wang, Liang-Kai, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Lai, Shih-Ting, Chang, Shun-Ping, Yang, Chien-Wen, Pan, Chen-Wen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.08.2017)
Published in Taiwanese journal of obstetrics & gynecology (01.08.2017)
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Journal Article
Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome
Chen, Chih-Ping, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Yen-Ni, Chen, Shin-Wen, Lee, Chen-Chi, Yang, Chien-Wen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.12.2016)
Published in Taiwanese journal of obstetrics & gynecology (01.12.2016)
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Journal Article
Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome
Chen, Chih-Ping, Hung, Fang-Yu, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Yen-Ni, Chen, Shin-Wen, Yang, Chien-Wen, Chen, Wen-Lin, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.04.2017)
Published in Taiwanese journal of obstetrics & gynecology (01.04.2017)
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Journal Article
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21
Chen, Chih-Ping, Chen, Ming, Chern, Schu-Rern, Chang, Shun-Ping, Chen, Shin-Wen, Lai, Shih-Ting, Chen, Wen-Lin, Lee, Meng-Shan, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.08.2017)
Published in Taiwanese journal of obstetrics & gynecology (01.08.2017)
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Journal Article
Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia
Chen, Chih-Ping, Lin, Shuan-Pei, Liu, Yu-Peng, Chern, Schu-Rern, Chen, Shin-Wen, Lai, Shih-Ting, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.06.2017)
Published in Taiwanese journal of obstetrics & gynecology (01.06.2017)
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Journal Article
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16
Chen, Chih-Ping, Ko, Tsang-Ming, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Lai, Shih-Ting, Yang, Chien-Wen, Pan, Chen-Wen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.08.2017)
Published in Taiwanese journal of obstetrics & gynecology (01.08.2017)
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Journal Article
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
Chen, Chih-Ping, Chen, Chen-Yu, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Lai, Shih-Ting, Chuang, Tzu-Yun, Yang, Chien-Wen, Chen, Li-Feng, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.12.2017)
Published in Taiwanese journal of obstetrics & gynecology (01.12.2017)
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Journal Article
Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities
Chen, Chih-Ping, Ko, Tsang-Ming, Wang, Liang-Kai, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Lai, Shih-Ting, Chuang, Tzu-Yun, Yang, Chien-Wen, Lee, Chen-Chi, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.02.2018)
Published in Taiwanese journal of obstetrics & gynecology (01.02.2018)
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Journal Article
Cyr61 Induces Gastric Cancer Cell Motility/Invasion via Activation of the Integrin/Nuclear Factor-κB/Cyclooxygenase-2 Signaling Pathway
Lin, Ming-Tsai, Zuon, Chung-Yaou, Chang, Cheng-Chi, Chen, Szu-Ta, Chen, Chih-Ping, Lin, Been-Ren, Wang, Ming-Yang, Jeng, Yung-Ming, Chang, King-Jen, Lee, Po-Huang, Chen, Wei-Jao, Kuo, Min-Liang
Published in Clinical cancer research (15.08.2005)
Published in Clinical cancer research (15.08.2005)
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Journal Article
Schimmelpenning Syndrome: A Case Report and Literature Review
Wang, Shwu-Meei, Hsieh, Ya-Ju, Chang, Kuo-Ming, Tsai, Hsiang-Ling, Chen, Chih-Ping
Published in Pediatrics and neonatology (01.12.2014)
Published in Pediatrics and neonatology (01.12.2014)
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Journal Article
Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality
Chen, Chih-Ping, Fu, Chung-Hu, Lin, Yi-Hui, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Yen-Ni, Chen, Shin-Wen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.12.2016)
Published in Taiwanese journal of obstetrics & gynecology (01.12.2016)
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Journal Article
Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome
Chen, Chih-Ping, Hung, Fang-Yu, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Yen-Ni, Chen, Shin-Wen, Lee, Meng-Shan, Yang, Chien-Wen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.12.2016)
Published in Taiwanese journal of obstetrics & gynecology (01.12.2016)
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Journal Article
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
Chen, Chih-Ping, Lin, Chen-Ju, Chen, Yen-Ni, Chern, Schu-Rern, Chen, Shin-Wen, Lai, Shih-Ting, Wu, Peih-Shan, Chen, Li-Feng, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.06.2017)
Published in Taiwanese journal of obstetrics & gynecology (01.06.2017)
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