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机构 日期 题名 作者
中國醫藥大學 2000 A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) causes non-syndromic craniosynostosis Tsai, FJ; Wu, JY; Lee, CC; Tsai, CH
中國醫藥大學 2000 Antley-Bixler syndrome associated with Arnold-Chiari malformation Chang, YT; Tsai, FJ; Shen, WC; Lin, HC; Peng, CT; Tsai, CH
中國醫藥大學 2000 Breech deformation complex in neonates Hsieh, YY; Tsai, FJ; Lin, CC; Chang, FCC; Tsai, CH
中國醫藥大學 2000 Breech deformation complex in neonates Hsieh, YY; Tsai, FJ; Lin, CC; Chang, FCC; Tsai, CH
中國醫藥大學 2000 Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency Lee, HH; Chang, JG; Tsai, CH; Tsai, FJ; Chao, HT; Chung, BC
中國醫藥大學 2000 Mutation analysis of thyroid peroxidase gene in Taiwanese patients with total iodide organification defects: Identification of five novel mutations. Wu, J; Yang, CF; Tsai, FJ
中國醫藥大學 2000 Aberrant transcripts of FHIT, TSG101 and PTEN/MMAC1 genes in normal peripheral mononuclear cells Wang, NM; Chang, JG; Liu, TC; Lin, SF; Peng, CT; Tsai, FJ; Tsai, CH
中國醫藥大學 2000 Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency Lee, HH; Chang, JG; Tsai, CH; Tsai, FJ; Chao, HT; Chung, BC
中國醫藥大學 1999 Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data Tsai, FJ; Tsai, CH; Chang, JG; Wu, JY
中國醫藥大學 1999 Identification of a common N540K mutation in 8/18 Taiwanese hypochondroplasia patients: further evidence for genetic heterogeneity Tsai, FJ; Wu, JY; Tsai, CH; Chang, JG
中國醫藥大學 1999 Bcl 10 is not commonly mutated in multiple primary solid tumors. Chang, JG; Lee, HH; Wang, NM; Yeh, KT; Tsai, FJ; Tsai, CH
中國醫藥大學 1999 Further characterization of Wilson disease in Taiwan: identification of two novel mutations and high correlation between haplotype and mutation. Wu, JY; Tsai, FJ; Lee, CC; Chang, JG; Tsai, CH
中國醫藥大學 1999 Different race, different face: minor anomalies in Chinese newborn infants Tsai, FJ; Tsai, CH; Peng, CT; Wu, JY; Lien, CH; Wang, TR
中國醫藥大學 1999 Prenatal diagnosis of dyssegmental dysplasia - A case report Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, FJ; Tsai, CH
中國醫藥大學 1999 Molecular analysis of secretor type alpha(1,2)-fucosyltransferase gene mutations in the Chinese and Thai populations Chang, JG; Yang, TY; Liu, TC; Lin, TP; Hu, CJ; Kao, MC; Wang, NM; Tsai, FJ; Peng, CT; Tsai, CH
中國醫藥大學 1999 Molecular analysis of secretor type alpha(1,2)-fucosyltransferase gene mutations in the Chinese and Thai populations Chang, JG; Yang, TY; Liu, TC; Lin, TP; Hu, CJ; Kao, MC; Wang, NM; Tsai, FJ; Peng, CT; Tsai, CH
中國醫藥大學 1999 Prenatal diagnosis of dyssegmental dysplasia - A case report Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, FJ; Tsai, CH
中國醫藥大學 1998 Mutation analysis in fibroblast growth factor receptor genes: Chinese data Lin, SP; Tsai, FJ; Wu, JY; Peng, CT; Tsai, CH
中國醫藥大學 1998 Mutation analysis of Chinese patients with Wilson disease Tsai, FJ; Wu, JY; Chang, JG; Lin, SP; Peng, CT; Tsai, CH
中國醫藥大學 1998 Molecular diagnosis of patients with beta-thalassemia major in central Taiwan by amplified created restriction site analysis Peng, CT; Wu, JY; Tsai, CH; Tsai, FJ; Chang, JG
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

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