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Showing items 216-225 of 257  (26 Page(s) Totally)
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Institution Date Title Author
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

Showing items 216-225 of 257  (26 Page(s) Totally)
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