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Showing items 2851-2875 of 7244. (290 Page(s) Totally) << < 110 111 112 113 114 115 116 117 118 119 > >> View [10|25|50] records per page

Date	Title	Authors
2012-06	Preliminary Study of the Application of PET Knitted Fabrics in Artificial Bone Scaffold	(Ching-Wen Lou); (Mei-Hui Li); (Wen-Cheng Chen)*; (Jin-Jia Hu); (Chao-Tsang Lu); 林佳弘(Jia-Horng Lin)*
1999-03	Preliminary Study of the Voice Characteristics of Yin-vacuity Patients	楊中賢(Chung-Hsion Yang); 張恆鴻*; 邱創乾; 陳瑞照; 卓家祥; 吳文祥; 羅綸謙(Lun-Chien Lo)
2008-06	Prenatal 3-Dimensional Sonographic and MRI Findings in Omphalocele–Exstrophy–Imperforate Anus–Spinal Defects Complex.	陳持平(Chih-Ping Chen)*; 張東曜(Tung-Yao Chang); 劉育鵬(Yu-Peng Liu); 蔡輔仁(Fuu-Jen Tsai); 簡淑錦(Shu-Chin Chien); 曹建銘(Chien-Ming Tsao); 楊曉白(Hsiao-Bai Yang); 王偉信(Wayseen Wang)
2009-02-28	prenatal detection of a de novo satellited Yp from the father carrying a satellited Xp as a possible result of an unstable translocation during Xp-Yp pairing	簡淑錦(Shu-Chin Chien); (Cheng-Tiao Hsieh PhD); 何銘(Ming- Ho); 林齊強(Chyi-Chyang Lin); 蔡輔仁(Fuu-Jen Tsai)*
2012-09	Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); (Jun-Wei Su); (Yu-Ting Chen); (Chen-Chi Lee); (Wayseen Wang)
2015-10	Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome and Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1	陳持平(Chih-Ping Chen)*; (Ming-Huei Lin); (Yi-Yung Chen); (Schu-Rern Chern); (Yen-Ni Chen); (Peih-Shan Wu); (Chen-Wen Pan); (Meng-Shan Lee); (Wayseen Wang)
2015-02	Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diap	陳持平(Chih-Ping Chen)*; (Yeou-Lih Wang); (Schu-Rern Chern); (Yu-Peng Liu); (Cheng-Ran Peng); (Yu-Ling Kuo); (Peih-Shan Wu); (Wen-Lin Chen); (Wayseen Wang)
2012-03	Prenatal diagnosis and genetic analysis of fetal akinesia deformation sequence and multiple pterygium syndrome associated with neuromuscular junction disorders: a review	陳持平(Chih-Ping Chen)*
2010-03	PRENATAL DIAGNOSIS AND GENETIC COUNSELING FOR MOSAIC TRISOMY 13	陳持平(Chih-Ping Chen)*
2007-03	Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome)	陳持平(Chih-Ping Chen)*; 林炫沛(Shuan-Pei Lin); 曾嶔元(Chin-Yuan Tzen); 胡務亮(Wuh-Liang Hwu); 陳樹人(Schu-Rern Chern); 莊志光(Chih-Kuang Chuang); 蔣淑清(Shu-Shien Chien); 王偉信(Wayseen Wang)
2005	Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3 -> qter) and partial trisomy 18q (18q23 -> qter) in a fetus associated with cystic hygroma and ambiguous genitalia	Chen, CP; Chern, SR; Wang, TH; Hsueh, DW; Lee, CC; Town, DD; Wang, WS; Ko, TM
2014-12	Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome	陳持平(Chih-Ping Chen)*; (Chen-Ju Lin); (Schu-Rern Chern); (Yu-Peng Liu); (Yu-Ling Kuo); (Peih-Shan Wu); (Dai-Dyi Town); (Li-Feng Chen); (Chien-Wen Yang); (Wayseen Wang)
2013-06	Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1->q31.1)	陳持平(Chih-Ping Chen)*; (Shing-Jyh Chang,); (Schu-Rern Chern); (Peih-Shan Wu); (Yu-Ting Chen); (Jun-Wei Su); (Wen-Lin Chen); (Wayseen Wang)
2013-03	Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3->q32.12) associated with abnormal maternal serum biochemistry	陳持平(Chih-Ping Chen)*; (Kwui-Shuai Hwang); (Her-Young Su); (Shuan-Pei Lin); (Yi-Ning Su); (Schu-Rern Chern); (Yu-Ting Chen); (Jun-Wei Su); (Wen-Lin Chen); (Wayseen Wang)
2013-12	Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Chen-Yu Chen); (Schu-Rern Chern); (Peih-Shan Wu); 蘇俊維(Jun-Wei Su); (Chen-Chi Lee); (Li-Feng Chen); (Wayseen Wang)
2011-09	Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Ming Chen); (Jain-Pei Huang); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Wen-Lin Chen); (Wayseen Wang)
2013-03	Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2->q11.21)	陳持平(Chih-Ping Chen)*; (Tsang-Ming Ko); (Yi-Ning Su); (Jun-Wei Su); (Yu-Ting Chen); (Chen-Chi Lee); (Li-Feng Chen); (Wayseen Wang)
2010-06	Prenatal diagnosis and molecular cytogenetic characterization of a small supermerary marker chromosome dericed from chromosome 18 and associated with a reciprocal translocation involving chromosome 17 and 18.	Chen)*, 陳持平(Chih-Ping; Lin), 林齊強(Chyi-Chyang
2010-02	Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18	陳持平(Chih-Ping Chen)*; (Chyi-Chyang Lin); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Yu-Ting Chen); (Schu-Rern Chern); (Chen-Chi Lee); (Dai-Dyi Town); (Li-Feng Chen); (Pei-Chen Wu); (Wayseen Wang)
2010-09	Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21	陳持平(Chih-Ping Chen)*; (Chyi-Chyang Lin); (Tsang-Ming Ko); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chen-Chi Lee); (Yu-Ting Chen); (Pei-Chen Wu); (Wayseen Wang)
2010-09	Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22	陳持平(Chih-Ping Chen)*; (Chyi-Chyang Lin); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chen-Chi Lee); (Wen-Ling Chen); (Li-Feng Chen); (Pei-Chen Wu); (Wayseen Wang)
2010-12	Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8	陳持平(Chih-Ping Chen)*; (Ming Chen); (Tsang-Ming Ko); (Gwo-Chin Ma); 蔡輔仁(Fuu-Jen Tsai); (Ming-Song Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Li-Feng Che); (Wayseen Wang)
2014-06	Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects	Yu-Ling Kuo; 陳持平(Chih-Ping Chen)*; (Liang-Kai Wang); (Tsang-Ming Ko); (Tung-Yao Chang); (Schu-Rern Chern); (Peih-Shan Wu); (Yu-Ting Chen); (Shu-Yuan Chang)
2013-03	Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21->qter) and partial monosomy 6q (6q27->qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold	陳持平(Chih-Ping Chen)*; (Yi-Yung Chen); (Schu-Rern Chern); (Peih-Shan Wu); (Jun-Wei Su); (Yu-Ting Chen); (Li-Feng Chen); (Wayseen Wang)
2010-09	Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3->pter) and partial monosomy 13q (13q33.3->qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly	陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chin-Yuan Hsu); (Pei-Chen Wu); (Dai-Dyi Town); (Dong-Jay Lee); (Gwo-Chin Ma); (Wayseen Wang)

Showing items 2851-2875 of 7244. (290 Page(s) Totally) << < 110 111 112 113 114 115 116 117 118 119 > >> View [10|25|50] records per page