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Showing items 316-325 of 327  (33 Page(s) Totally)
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Institution Date Title Author
中國醫藥大學 1998 Prenatal diagnosis of Apert syndrome Chang, CC; Tsai, FJ; Tsai, HD; Tsai, CH; Hsieh, YY; Lee, CC; Yang, TC; Wu, JY
中國醫藥大學 1998 Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with apert syndrome Tsai, FJ; Hwu, WL; Lin, SP; Chang, JG; Wang, TR; Tsai, CH
中國醫藥大學 1998 Molecular analysis of type I oculocutaneous albinism in Chinese Wu, JY; Lin, SP; Tsai, LP; Tsai, FJ; Peng, CT; Tsai, CH
中國醫藥大學 1998 Rotavirus associated with poliomyelitis-like syndrome Chou, IC; Tsai, CH; Tsai, FJ
中國醫藥大學 1998 Myelination arrest demonstrated using magnetic resonance imaging in a child with type I G(M1) gangliosidosis Shen, WC; Tsai, FJ; Tsai, CH
中國醫藥大學 1997 Mutations in fibroblast growth factor receptor genes: Chinese data. Tsai, FJ; Wu, JY; Peng, CT; Tsai, CH
中國醫藥大學 1996 Catabolic effect in premature infants with early dexamethasone treatment Tsai, FJ; Tsai, CH; Wu, SF; Liu, YH; Yeh, TF
中國醫藥大學 1996 Detection of congenital cytomegalovirus infection in Chinese newborn infants using polymerase chain reaction Tsai, CH; Tsai, FJ; Shih, YT; Wu, SF; Liu, SC; Tseng, YH
中國醫藥大學 1996 X-linked recessive myotubular myopathy proven by muscle biopsy Tsai, CH; Huang, WS; Tsai, FJ; Lee, CC; Chen, SS
中國醫藥大學 1996 X-linked recessive myotubular myopathy proven by muscle biopsy Tsai, CH; Huang, WS; Tsai, FJ; Lee, CC; Chen, SS

Showing items 316-325 of 327  (33 Page(s) Totally)
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