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教育部委託研究計畫      計畫執行:國立臺灣大學圖書館
 
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機構 日期 題名 作者
中國醫藥大學 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
中國醫藥大學 2003 Insulin-like growth factor-II gene polymorphism is associated with primary open angle glaucoma Tsai, FJ; Lin, HJ; Chen, WC; Chen, HY; Fan, SS
中國醫藥大學 2002 Characterization of four novel b-galactosidase gene mutations and a polymorphism in Taiwanese patients with GMI-gangliosidosis. Wu, JY; Yang, CF; Tsai, FJ
中國醫藥大學 2002 Association between angiotensinogen gene M235T polymorphism and mitral valve prolapse syndrome in Taiwan Chinese Chou, HT; Hung, JS; Chen, YT; Shi, YR; Tsai, FJ
中國醫藥大學 2002 Lack of association between transforming growth factor-beta 1 gene polymorphisms and mitral valve prolapse in Taiwan Chinese Chou, HT; Shi, YR; Hsu, Y; Tsai, FJ
中國醫藥大學 2002 Correlation of p21 gene codon 31 polymorphism and TNF-alpha gene polymorphism with nasopharyngeal carcinoma Tsai, MH; Chen, WC; Tsai, FJ
中國醫藥大學 2002 Cytochrome P450c17 alpha (CYP17) gene polymorphism is not associated with leiomyoma susceptibility Hsieh, YY; Tsai, FJ; Chang, CC; Tsai, CH; Lin, CC; Yeh, LS
中國醫藥大學 2002 The polymorphisms of codon 727 and 52 of thyroid-stimulating hormone receptor gene are not associated with mitral valve prolapse syndrome in Taiwan Chinese Chou, HT; Shi, YR; Chang, CT; Tsai, FJ
中國醫藥大學 2002 Smith-Magenis syndrome with bilateral vesicoureteral reflux: A case report Chou, IC; Tsai, FJ; Yu, MT; Tsai, CH
中國醫藥大學 2002 Interleukin-4 intron 3 polymorphism is not related to susceptibility to febrile seizures Tsai, FJ; Chou, IC; Hsieh, YY; Lee, CC; Lin, CC; Tsai, CH
中國醫藥大學 2002 Polymorphisms for interleukin 1 beta exon 5 and interleukin 1 receptor antagonist in Taiwanese children with febrile convulsions Tsai, FJ; Hsieh, YY; Chang, CC; Lin, CC; Tsai, CH
中國醫藥大學 2002 Polymorphisms for interleukin-4 (IL-4)-590 promoter, IL-4 intron3, and tumor necrosis factor alpha-308 promoter: Non-association with endometriosis Hsieh, YY; Chang, CC; Tsai, FJ; Hsu, Y; Tsai, HD; Tsai, CH
中國醫藥大學 2002 Angiotensin h type 1 receptor gene adenine/cytosine(1166) polymorphism is not associated with mitral valve prolapse syndrome in Taiwan Chinese Chou, HT; Shi, YR; Wu, JY; Tsai, FJ
中國醫藥大學 2002 The proline form of p53 codon 72 polymorphism is associated with endometriosis Chang, CC; Hsieh, YY; Tsai, FJ; Tsai, CH; Tsai, HD; Lin, CC
中國醫藥大學 2002 Urokinase gene 3 '-UTR T/C polymorphism is associated with urolithiasis Tsai, FJ; Lin, CC; Lu, HF; Chen, HY; Chen, WC
中國醫藥大學 2002 Urokinase gene 3 '-UTR T/C polymorphism is associated with urolithiasis Tsai, FJ; Lin, CC; Lu, HF; Chen, HY; Chen, WC
中國醫藥大學 2002 A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tarda Shi, YR; Lee, CC; Hsu, YA; Wang, CH; Tsai, FJ
中國醫藥大學 2002 A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tarda Shi, YR; Lee, CC; Hsu, YA; Wang, CH; Tsai, FJ
中國醫藥大學 2002 Interleukin-1 receptor antagonist gene polymorphism in Chinese patients with systemic lupus erythematosus Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學 2002 Interleukin-1 receptor antagonist gene polymorphism in Chinese patients with systemic lupus erythematosus Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學 2002 Distributions of p53 codon 72 polymorphism in primary open angle glaucoma Lin, HJ; Chen, WC; Tsai, FJ; Tsai, SW
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 No association of vitamin D receptor gene start codon Fok I 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 2002 Mutation analysis of thyroid peroxidase gene in Chinese patients with total iodide organification defect: Identification of five novel mutations Wu, JY; Shu, SG; Yang, CF; Lee, CC; Tsai, FJ

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