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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 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
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 Prognostic significance of the proline form of p53 codon 72 polymorphism in nasopharyngeal carcinoma Tsai, MH; Lin, CD; Hsieh, YY; Chang, FCC; Tsai, FJ; Chen, WC; Tsai, CH
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 Turner syndrome with pseudodicentric Y chromosome mosaicism Hsieh, YY; Lin, WC; Chang, CC; Tsai, FJ; Yu, MT; Tsai, HD; Tsai, CH
中國醫藥大學 2002 Turner syndrome with pseudodicentric Y chromosome mosaicism Hsieh, YY; Lin, WC; Chang, CC; Tsai, FJ; Yu, MT; Tsai, HD; Tsai, CH
中國醫藥大學 2002 p21 gene codon 31 polymorphism is associated with bladder cancer Chen, WC; Wu, HC; Hsu, CD; Chen, HY; Tsai, FJ
中國醫藥大學 2002 Relation of vitamin D receptor FokI start codon polymorphism. to bone mineral density and occurrence of osteoporosis in postmenopausal women in Taiwan Chen, HY; Chen, WC; Hsu, CD; Tsai, FJ; Tsai, CH
中國醫藥大學 2002 Molecular analysis of thiopurine S-methyltransferase alleles in South-east Asian populations Chang, JG; Lee, LS; Chen, CM; Shih, MC; Wu, MC; Tsai, FJ; Liang, DC
中國醫藥大學 2002 Unstable Hb Perth in a Taiwanese subject: A T -> C substitution at codon 32 of the beta-globin gene creates an MspI site Chang, JG; Liu, HC; Shih, MC; Liu, SC; Chan, WL; Tsai, FJ
中國醫藥大學 2002 Unstable Hb Perth in a Taiwanese subject: A T -> C substitution at codon 32 of the beta-globin gene creates an MspI site Chang, JG; Liu, HC; Shih, MC; Liu, SC; Chan, WL; 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 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

顯示項目 221-245 / 327 (共14頁)
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