馬偕醫學院機構典藏(Mackay Medical College Institutional Repository):Items for Author
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Items for Author "Hsien-Hsiung Lee" 

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Showing 10 items.

Collection Date Title Authors Bitstream
[生物醫學研究所] 期刊論文 2006-12-01 Use of a PCR-based amplification analysis as a substitute for the Southern blot method to determine the C4A and C4B genes Hsien-Hsiung Lee; Yung-Te Tseng; Yann-Jinn Le
[生物醫學研究所] 期刊論文 2006-10-01 Identification of the size and antigenic determinants of the human C4 gene by a polymerase chain-reaction-based amplification method Hsien-Hsiung Lee; Shwu-Fen Chang; Yung-Te Tseng; Yann-Jinn Lee
[生物醫學研究所] 期刊論文 2006-08-01 Diversity of the CYP21A2 gene: A 6.2-kb TaqI fragment and a 3.2-kb TaqI fragment mistaken as CYP21A1P Hsien-Hsiung Lee; Fuu-Jen Tsai; Yann-Jinn Lee; Yuh-Cheng Yang
[生物醫學研究所] 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
[生物醫學研究所] 期刊論文 2005-04-01 Novel missense mutations, GCC [Ala306]- > GTC [Val] and ACG [Thr318]- > CCG [Pro], in the CYP11B1 gene cause steroid 11beta-hydroxylase deficiency in the Chinese Hsien-Hsiung Lee; Ging-Shing Won; Hsiang Tai Chao; Yann-Jinn Lee; Bon-Chu Chung
[生物醫學研究所] 期刊論文 2004-06-01 Use of PCR-based amplification analysis as a substitute for the Southern blot method for CYP21 deletion detection in congenital adrenal hyperplasia Hsien-Hsiung Lee; Yann-Jinn Lee; Peter Chan; Ching-Yu Lin
[生物醫學研究所] 期刊論文 2004-05-01 PCR-based detection of the CYP21 deletion and TNXA/TNXB hybrid in the RCCX module Hsien-Hsiung Lee; Yann-Jinn Lee; Ching-Yu Lin
[生物醫學研究所] 期刊論文 2003-12-01 Molecular identification of combined homozygous and compound heterozygous mutations in the CYP21 gene in simple virilizing congenital adrenal hyperplasia in Taiwan Hsu-Hui Wang; Hsien-Hsiung Lee; Du-An Wu; Yann-Jin Lee; Bon-Chu Chung; Tso-Ren Wang
[生物醫學研究所] 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
[生物醫學研究所] 期刊論文 2000-02-01 Carrier analysis and prenatal diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in Chinese Hsien-Hsiung Lee; Jing-Mei Kuo; Hsiang-Tai Chao; Yann-Jinn Lee; Jan-Gowth Chang; Chang-Hai Tsai; Bon-chu Chung

 


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