English  |  正體中文  |  简体中文  |  总笔数 :0  
造访人次 :  51741795    在线人数 :  1099
教育部委托研究计画      计画执行:国立台湾大学图书馆
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
关于TAIR

浏览

消息

著作权

相关连结

"wu jy"的相关文件

回到依作者浏览
依题名排序 依日期排序

显示项目 201-225 / 257 (共11页)
<< < 2 3 4 5 6 7 8 9 10 11 > >>
每页显示[10|25|50]项目

机构 日期 题名 作者
中國醫藥大學 2002 Association of vitamin D receptor gene BsmI polymorphisms in Chinese patients with systemic lupus erythematosus Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學 2002 Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學 2002 Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學 2002 Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學 2002 Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學 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
中國醫藥大學 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
中國醫藥大學 2002 Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers Lin, WD; Wu, JY; Tsai, FJ; Gau, MT; Lee, CC
中國醫藥大學 2002 Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers Lin, WD; Wu, JY; Tsai, FJ; Gau, MT; Lee, CC
中國醫藥大學 2002 Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method Shi, YR; Hsieh, KS; Wu, JY; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學 2002 Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome Wang, TJ; Huang, CB; Tsai, FJ; Wu, JY; Lai, RB; Hsiao, M
中國醫藥大學 2002 Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome Wang, TJ; Huang, CB; Tsai, FJ; Wu, JY; Lai, RB; Hsiao, M
中國醫藥大學 2002 Association of vitamin D receptor gene BsmI polymorphisms in Chinese patients with systemic lupus erythematosus Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學 2002 Lack of association of interleukin-1 beta gene polymorphisms in Chinese patients with systemic lupus erythematosus Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學 2001 Androgen receptor trinucleotide polymorphism in endometriosis Hsieh, YY; Chang, CC; Tsai, FJ; Wu, JY; Tsai, CH; Tsai, HD
中國醫藥大學 2001 Molecular analysis of GM1-gangliosidosis: identification and characterization of four novel mutations in two Taiwan Chinese patients. Tsai, FJ; Yang, CF; Wu, JY
中國醫藥大學 2001 Further evidence that fibroblast growth factor receptor 2 mutations cause Antley-Bixler syndrome Tsai, FJ; Wu, JY; Yang, CF; Tsai, CH
中國醫藥大學 2001 Molecular analysis of two patients with 3-hydroxy-methyl-glutaric aciduria: identification of three novel mutations including one de novo mutation. Wu, JY; Yang, CF; Tsai, FJ
中國醫藥大學 2001 Relation of polymorphism in the promotor region for the human osteocalcin gene to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan Chen, HY; Tsai, HD; Chen, WC; Wu, JY; Tsai, FJ; Tsai, CH
中國醫藥大學 2001 Polymorphisms for interleukin-1 beta (IL-1 beta)-511 promoter, IL-1 beta exon 5, and IL-1 receptor antagonist: Nonassociation with endometriosis Hsieh, YY; Chang, CC; Tsai, FJ; Wu, JY; Shi, YR; Tsai, HD; Tsai, CH
中國醫藥大學 2001 Osteocalcin gene Hind III polymorphism is not correlated with calcium oxalate stone disease Chen, WC; Chen, HY; Wu, JY; Chen, YT; Tsai, FJ
中國醫藥大學 2001 Osteocalcin gene Hind III polymorphism is not correlated with calcium oxalate stone disease Chen, WC; Chen, HY; Wu, JY; Chen, YT; Tsai, FJ
中國醫藥大學 2001 Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients Tsai, FJ; Yang, CF; Wu, JY; Tsai, CH; Lee, CC
中國醫藥大學 2001 Interleukin-1 beta and interleukin-1 receptor antagonist gene polymorphisms in rheumatoid arthritis Huang, CM; Tsai, FJ; Wu, JY; Wu, MC
中國醫藥大學 2001 Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele Hsieh, YY; Wu, JY; Chang, CC; Tsai, FJ; Lee, CC; Tsai, HD; Tsai, CH

显示项目 201-225 / 257 (共11页)
<< < 2 3 4 5 6 7 8 9 10 11 > >>
每页显示[10|25|50]项目