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类别 日期 题名 作者 档案
[生物醫學研究所] 期刊論文 2011-05-01 Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene Chia-Cheng Hung; Shin-Yu Lin; Chien-Nan Lee; Chih-Ping Chen; Shuan-Pei Lin; Mei-Chyn Chao; Shyh-Shin Chiou; Yi-Ning Su
[醫學系] 期刊論文 2007-03-01 Prader-Willi syndrome in Taiwan Hsiang-Yu Lin; Shuan-Pei Lin; Jui-Lung Yen; Yann-Jinn Lee; Chi-Yu Huang; Han-Yang Hung; Chyong-Hsin Hsu; Hsin-An Kao; Jui-Hsing Chang; Nan-Chang Chiu; Che-Sheng Ho; Mei-Chyn Chao; Dan-Ming Niu; Li-Ping Tsai; Pao-Lin Kuo
[醫學系] 期刊論文 2006-02-01 Only two amino acid substitutions of I236N and V237E in exon 6 are converted to the CYP21 gene in a Chinese patient with congenital adrenal hyperplasia Hsien-Hsiung Lee; Mei-Chyn Chao; Yann-Jinn Lee
[醫學系] 期刊論文 1998-03-01 Identification of four novel mutations in the CYP21 gene in congenital adrenal hyperplasia in the Chinese H.-H. Lee; Hsiang-Tai Chao; Yann-Jinn Lee; San-Ging Shu; Mei-Chyn Chao; Jing-Mei Kuo; Bun-chu Chung
[醫學系] 期刊論文 2007-06-01 Genotype and phenotype in patients with Prader-Willi syndrome in Taiwan Hsiang-Yu Lin; Shuan-Pei Lin; Chih-Kuang Chuang; Ming-Ren Chen; Jui-Lung Yen; Yann-Jinn Lee; Chi-Yu Huang; Li-Ping Tsai; Dau-Ming Niu; Mei-Chyn Chao; Pao-Lin Kuo
[醫學系] 期刊論文 2003-02-01 Deletion of the C4-CYP21 repeat module leading to the formation of a chimeric CYP21P/CYP21 gene in a 9.3-kb fragment as a cause of steroid 21-hydroxylase deficiency Hsien-Hsiung Lee; Shwu-Fen Chang; Yann-Jinn Lee; Salmo Raskin; Shio-Jean Lin; Mei-Chyn Chao; Fu-Sung Lo; Ching-Yu Lin

 

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