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Showing items 301-310 of 327 (33 Page(s) Totally)
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| 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.
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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
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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
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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
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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
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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.
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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.
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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
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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
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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
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Chang, JG; Yang, TY; Liu, TC; Lin, TP; Hu, CJ; Kao, MC; Wang, NM; Tsai, FJ; Peng, CT; Tsai, CH |
Showing items 301-310 of 327 (33 Page(s) Totally)
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