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Showing items 296-305 of 327  (33 Page(s) Totally)
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Institution Date Title Author
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

Showing items 296-305 of 327  (33 Page(s) Totally)
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