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臺灣機構典藏 TAIR >  依作者瀏覽

"shuan pei lin"的相關文件

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機構 日期 題名 作者
臺大學術典藏 2021-07-14T03:36:13Z The Ethics and Guidelines of Next-Generation Sequencing Genetic Testing and Counseling DANIEL FU-CHANG TSAI; Yu-Chen Juang; Yin-Hsiu Chien; Ni-Chung Lee; Hung Chih-Yu Wang; Shuan-Pei Lin; Wuh-Liang Hwu
中國醫藥大學 2015-05-17 Molecular Aspects of Mucopolysaccharidosis IVA in Taiwan 林瑋德(Wei-De Lin);周宜卿(I-Ching Chou);(Shuan-Pei Lin);(Pao-Chin Chiu);(Wuh-Liang Hwu);王仲興(Chung-Hsing Wang);蔡輔仁(Fuu-Jen Tsai)*
國立交通大學 2014-12-13T10:40:08Z 唇顎製成因之探討---轉化性生長因子α(TGFA)之遺傳與唇顎裂發生之關聯性研究 林炫沛; Shuan-Pei Lin
亞洲大學 2014-03 A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation Chih-Ping Chen;Shuan-Pei Lin;Schu-Rern Chern;Peih-Shan Wu;Jun-Wei Su;Chen-Chi Lee; Wayseen Wang
亞洲大學 2014-03 Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes Chih-Ping Chen;Pu-Tsui Wang;Shuan-Pei Lin;Schu-Rern Chern;Yu-Ting Chen;Peih-Shan Wu;Yu-Ling Kuo;Wen-Lin Chen;Wayseen Wang
中國醫藥大學 2014-03 A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation 陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Schu-Rern Chern);(Peih-Shan Wu);蘇俊維(Jun-Wei Su);(Chen-Chi Lee);(Wayseen Wang)
中國醫藥大學 2014-03 Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes 陳持平(Chih-Ping Chen)*;(Pu-Tsui Wang);(Shuan-Pei Lin);(Schu-Rern Chern);(Yu-Ting Chen);(Peih-Shan Wu);(Yu-Ling Kuo);(Wen-Lin Chen);(Wayseen Wang)
中國醫藥大學 2013-07 6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia, psychomotor developmental delay and poor wound healing 陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yu-Peng Liu);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Jun-Wei Su);(Chen-Chi Lee);(Wayseen Wang)
中國醫藥大學 2013-06 A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 gene 陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Wayseen Wang)
中國醫藥大學 2013-06 Effects of Enzyme Replacement Therapy for Cardiac type Fabry Patients with a Chinese Hotspot Late-onset Fabry Mutation (IVS4+919G>A) (Hsiang-Yu Lin);(Hao-Chuan Liu);(Yu-Hsiu Huang);(Hsuan-Chieh Liao);(Ting-Rong Hsu);(Chia-I Shen);(Shao-Tzu Li);(Cheng-Fang Li);(Li-Hong Lee);(Pi-Chang Lee);(Chun-Kai Huang);(Chuan-Chi Chiang);林清淵(Ching-Yuang Lin);(Shuan-Pei Lin);(Dau-Ming Niu)*

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