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Date	Title	Authors
2003	Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency	Lee, HH; Chang, SF; Tsai, FJ; Tsai, LP; Lin, CY
2003-06	Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency.	(Lee HH); (Chang SF); 蔡輔仁(Fuu-Jen Tsai); (Tsai LP); (Lin CY)
2003-06	Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency.	(Lee HH); (Chang SF); 蔡輔仁(Fuu-Jen Tsai); (Tsai LP); (Lin CY)
2002	Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan	施怡如(Shi YR); 鄔哲源; (Hsu YA); 李正淳(Cheng-Chun Lee); 蔡長海(Chang-Hai Tsai); 蔡輔仁(Fuu-Jen Tsai)*
2002	Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan	Shi, YR; Wu, JY; Hsu, YA; Lee, CC; Tsai, CH; Tsai, FJ
2002	Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan	Shi, YR; Wu, JY; Hsu, YA; Lee, CC; Tsai, CH; Tsai, FJ
2013-07	Mutational analysis of the 5’ non-coding region of GJB1 in a Taiwanese cohort with Charcot-Marie-Tooth neuropathy	(Tsai PC); (Chen CH); (Liu AB); (Chen YC); (Soong BW); (Lin KP); 林秀芳(Shaw-Fang Yet); (Lee YC)*
2002	Mutational analysis of the autoprocessing site of subtilisin YaB-G124A	Chang, YS; Liaw, SH; Mei, HC; Hsu, CC; Wu, CY; Tsai, YC
2003-06	Mutational Analysis of the Melanocortin-4 Receptor Gene in Chinese Children with Obesity	林正介(Cheng-Chieh Lin); 劉秋松(Chiu-Shong Liu); 王妙媛(Nancy M. Wang); 陳志玫(Chih-Mei Chen); 李采娟(Tsai-Chung Li); 許世寬(Shih-Kuan Hsu); 陳偉德(Walter Chen)*
2004	Mutational, epigenetic and expressional analyses of caveolin-1 gene in breast cancers	Chen, ST; Lin, SY; Yeh, KT; Ku, SJ; Chan, WL; Chu, YP; Chang, JG

Showing items 17991-18000 of 54961. (5497 Page(s) Totally)
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