臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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	2019臺灣學術機構典藏研討會
	機構典藏系統RC7版本已發佈

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Institution	Date	Title	Author
中國醫藥大學	2011-05	RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia	林瑋德(Wei-De Lin); 林炫沛(Shuan-Pei Lin); 王仲興(Chung-Hsing Wang); 蔡育勳(Yuhsin Tsai); 陳持平(Chih-Ping Chen); 蔡輔仁(Fuu-Jen Tsai)*
中國醫藥大學	2010-04	FOXL2 mutations in Taiwanese patients with blepharophimosis, ptosis, epicanthus inversus syndrome.	林瑋德(Wei-De Lin); 周宜卿(I-Ching Chou); 李妮鐘(Ni-Chung Lee); 王仲興(Chung-Hsing Wang); 胡務亮; 林炫沛(Shuan-Pei Lin); 趙美琴(Mei-Chyn Chao); 蔡育勳(Yuhsin Tsai); 蔡輔仁(Fuu-Jen Tsai)*
中國醫藥大學	2009-06-10	FOXL2 mutations in Taiwanese patients with blepharophimosis-ptosis-epicanthus inversus syndrome	周宜卿(I-Ching Chou); 林瑋德(Wei-De Lin); 李妮鐘(Ni-Chung Lee); 王仲興(Chung-Hsing Wang); 郭煌宗(Haung-Tsung Kuo); 蔡長海(Chang-Hai Tsai); 林炫沛(Shuan-Pei Lin); 趙美琴(Mei-Chyn Chao); 胡務亮(Wuh-Liang Hwu); 蔡輔仁(Fuu-Jen Tsai)*
中國醫藥大學	2009-04-25	FOXL2 mutations in Taiwanese patients with blepharophimosis-ptosis-epicanthus inversus syndrome	周宜卿(I-Ching Chou); 林瑋德(Wei-De Lin); 李妮鐘(Ni-Chung Lee); 王仲興(Chung-Hsing Wang); 郭煌宗(Haung-Tsung Kuo); 蔡長海(Chang-Hai Tsai); 林炫沛(Shuan-Pei Lin); 趙美琴(Mei-Chyn Chao); 胡務亮(Wuh-Liang Hwu); 周宜卿(I-Ching Chou); 蔡輔仁(Fuu-Jen Tsai)*
中國醫藥大學	2008-06	Effects of Growth Hormone Treatment on Height, Weight, and obesity in Taiwanese Patients with Prader-Willi Syndrome.	林翔宇(Hsiang-Yu Lin); 林炫沛(Shuan-Pei Lin); 蔡立平(Li-Ping Tsai); 趙美琴(Mei-Chyn Chao); 陳銘仁(Ming-Ren Chen); 莊志光(Chin-Kuang Chuang); 黃琪鈺(Chi-Yu Huang); 蔡輔仁(Fuu-Jen Tsai); 周宜卿(I-Ching Chou); 邱寶琴(Pao-Ching Chiu); 黃正宏(Cheng-hung huang); 顏瑞龍(Jui-Lung Yen); 林如立(Ju-Li Len); 郭保麟(Pao-Lin Kuo)
中國醫藥大學	2007-09	Human Gene Mutations. Gene symbol: EXT1. Disease: exostoses (multiple) 1.	林瑋德(Wei-De Lin); 林炫沛(Shuan-Pei Lin); 陳持平(Chih-Ping Chen); 蔡輔仁(Fuu-Jen Tsai)*
中國醫藥大學	2007-04	台灣鎖骨顱骨發育不良症病患RUNX2基因分析之研究	王仲興(Chung-Hsing Wang); 林瑋德(Wei-De Lin); 林炫沛(Shuan-Pei Lin); 蔡長海(Chang-Hai Tsai); 蔡輔仁(Fuu-Jen Tsai)
中國醫藥大學	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)
中國醫藥大學	2006.12	Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: application in prader–Willi syndrome and duchenne muscular dystrophy	洪加政(Chia-Cheng Hung); 陳持平(Chih-Ping Chen); 林炫沛(Shuan-Pei Lin); 簡淑錦(Shu-Chin Chien); 李建南(Chien-Nan Lee); 鄭文芳(Wen-Fang Cheng); 謝武勳(Wu-Shiun Hsieh); 劉明松(Ming S. Liu); 蘇怡寧(Yi-Ning Su)*; 林文浬(Win-Li Lin)
中國醫藥大學	2006-12	24 Mb deletion of 6q22.1->q23.2 in an infant with pulmonary atresia, ventricular septal defect, microcephaly, developmental delay and facial dysmorphism	陳持平(Chih-Ping Chen)*; 王子豪(Tzu-Hao Wang); 林炫沛(Shuan-Pei Lin); 陳樹人(Schu-Rern Chern); 陳明仁(Ming-Ren Chen); 李貞姬(Chen-Chi Lee); 陳彥君(Yen-Jiun Chen); 王偉信(Wayseen Wang)

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