Items for Author "Chang, Tung-Yao"
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Showing 22 items.
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| [生物科技學系] 期刊論文 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q ; of paternal origin in a pregnancy with fetal cystic hygroma |
; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2009-12 |
Prenatal diagnosis of monosomy 17p (17p13.3->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly and Miller-Dieker lissencephaly syndrome in a fetus |
; Lin, Chin-Yi; 陳持平; Chen, Chih-Ping; Liau, Chiung-Ling; Su, Pen-Hua; Tsao, Teng-Fu; Chang, Tung-Yao; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-02 |
Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion |
Chen, Yen-Ni; Chen, Yen-Ni; 陳持平*; Tsang-Ming, K; Ko, Tsang-Ming; Wa, Liang-Kai; Wang, Liang-Kai; Wu, Pei-Chen; Wu, Pei-Chen; Cha, Tung-Yao; Chang, Tung-Yao; Wu, Peih-Shan; Wu, Peih-Shan; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-02 |
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 |
陳持平; Chen, Chih-Ping; *; Cha, Tung-Yao; Chang, Tung-Yao; Lin, Tan-Wei; Lin, Tan-Wei; Ch, Schu-Rern; Chern, Schu-Rern; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-06 |
22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae and congenital heart defects on prenatal ultrasound |
陳持平; Chen, Chih-Ping; *; Cha, Tung-Yao; Chang, Tung-Yao; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Chen, Weu-Lin; Chen, Weu-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-10 |
Prenatal imaging findings of a rapidly involuting congenital hemangioma (RICH) over right flank in a fetus with a favorable outcome |
陳持平; Chen, Chih-Ping; *; Chen, Chen-Yu; Chen, Chen-Yu; Cha, Tung-Yao; Chang, Tung-Yao; Yang, Hsiu-Yu; Yang, Hsiu-Yu; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-02 |
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 |
陳持平; Chen, Chih-Ping; *; Tsang-Ming, K; Ko, Tsang-Ming; Cha, Tung-Yao; Chang, Tung-Yao; Ch, Schu-Rern; Chern, Schu-Rern; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-10 |
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 |
陳持平; Chen, Chih-Ping; Cha, Shu-Yuan; Chang, Shu-Yuan; Wa, Liang-Kai; Wang, Liang-Kai; Cha, Tung-Yao; Chang, Tung-Yao; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, hin-Wen; Chen, hin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Ya, Chien-Wen; Yang, Chien-Wen |
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| [生物科技學系] 期刊論文 |
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Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of |
陳持平; Chen, Chih-Ping; Cha, Tung-Yao; Chang, Tung-Yao; Guo, Wan-Yuo; Guo, Wan-Yuo; Su, Yi-Ning; Su, Yi-Ning; Chen, Yi-Yung; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2017-12 |
Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound |
陳持平; Chen, Chih-Ping; Cha, Tung-Yao; Chang, Tung-Yao; Hung, Fang-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Lee, Chen-Chi; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs and thanatophoric dysplasia type II |
陳持平; Chen, Chih-Ping; Cha, Tung-Yao; Chang, Tung-Yao; Li, Ming-Huei; Lin, Ming-Huei; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2008-03 |
CONCOMITANT OMPHALOCELE AND ANENCEPHALY ASSOCIATED WITH TRISOMY 18 AND ARTHROGRYPOSIS DIAGNOSED IN EARLY PREGNANCY |
陳持平; Chen, Chih-Ping; Chang, Tung-Yao; Lin, Hung-Hung; Chern, Schu-Rern; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2013-04 |
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization |
陳持平; Chen, Chih-Ping; Lin, Chen-Ju; Lin, Chen-Ju; Cha, Tung-Yao; Chang, Tung-Yao; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yu-Ting; Chen, Yu-Ting; Su, Jun-Wei; Su, Jun-Wei; Lee, Chen-Chi; Lee, Chen-Chi; Chen, Li-Feng; Chen, Li-Feng; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2010-09 |
Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy |
陳持平; Chen, Chih-Ping; Liu, Yu-Peng; Chang, Tung-Yao; Tsai, Fuu-Jen; Chen, Chen-Yu; Wu, Pei-Chen; Chen, Teresa Hsiao-Tien; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2009-12 |
Prenatal diagnosis of a 22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect by array comparative genomic hybridization |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Chang, Tung-Yao; Chern, Schu-Rern; Tsai, Fuu-Jen; Hwang, Jonathan Kwei; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2010-09 |
Prenatal diagnosis of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Chang, Tung-Yao; Liu, Yu-Peng; Tsai, Fuu-Jen; Chen, Ming-Ren; Hwang, Jonathan Kwei; Chen, Teresa Hsiao-Tien; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2009-09 |
Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Chang, Tung-Yao; Liu, Yu-Peng; Tsai, Fuu-Jen; Hwang, Jonathan Kwei; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2014-03 |
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Su, Yi-Ning; Che, Shee-Uan; Chen, Shee-Uan; Cha, Tung-Yao; Chang, Tung-Yao; Wu, Pei-Chen; Wu, Pei-Chen; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Kuo, Yu-Ling; Kuo, Yu-Ling; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2009-03 |
PRENATAL DIAGNOSIS OF 46,XX,DER(13;21)(Q10;Q10),+21 AND TRANSIENT ABNORMAL MYELOPOIESIS IN A FETUS WITH HEPATOSPLENOMEGALY AND SPONTANEOUS RESOLUTION OF FETAL ASCITES |
陳持平; Chen, Chih-Ping; Tsai, Fuu-Jen; Chern, Schu-Rern; Chang, Tung-Yao; Hsu, Chin-Yuan; Lin, Hung-Hung; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome ;13q;13q; of paternal origin in a pregnancy with fetal cystic hygroma |
陳持平; Tsang-Ming, K; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma |
陳持平*; Tsang-Ming, K; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Detection of de novo secondary trisomy 13 due to isochromosome ;13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma |
陳持平*、Tsang-Ming, K; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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