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Showing items 286-295 of 327  (33 Page(s) Totally)
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Institution Date Title Author
中國醫藥大學 2001 Association of the vitamin D receptor gene start codon Fok I polymorphism with calcium oxalate stone disease Chen, WC; Chen, HY; Lu, HF; Hsu, CD; 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 2000 Mutation analysis of type 2 Gaucher disease in Taiwan Chinese and identification of two novel mutations. Tsai, FJ; Wu, JY; Lin, SP; Chang, JG; Lee, CC; Tsai, CH
中國醫藥大學 2000 Molecular analysis of syndromic congenital heart disease by using short tandem-repeat polymorphic markers. Shi, YR; Hsieh, KS; Wu, JY; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學 2000 Molecular analysis of the N-acetylgalactosamina-6-sulfate sulfatase gene in Taiwanese patients with Mucopolysaccharidosis IVA. Yang, CF; Tsai, FJ; Lin, SP; Wu, JY
中國醫藥大學 2000 Cytogenetic study of workers exposed to chromium compounds Wu, FY; Tsai, FJ; Kuo, HW; Tsai, CH; Wu, WY; Wang, RY; Lai, JS
中國醫藥大學 2000 Distributions of p53 codon 72 polymorphism in bladder cancer - proline form is prominent in invasive tumor Chen, WC; Tsai, FJ; Wu, JY; Wu, HC; Lu, HF; Li, CW
中國醫藥大學 2000 A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia Tsai, FJ; Wu, JY; Lin, WD; Tsai, CH
中國醫藥大學 2000 Infantile form G(M1) gangliosidosis with dilated cardiomyopathy: a case report Lin, HC; Tsai, FJ; Shen, WC; Tsai, CH; Peng, CT

Showing items 286-295 of 327  (33 Page(s) Totally)
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