|
"tsai fj"的相關文件
顯示項目 296-305 / 327 (共33頁)
<< < 24 25 26 27 28 29 30 31 32 33 > >>
每頁顯示[10|25|50]項目
| 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 |
顯示項目 296-305 / 327 (共33頁)
<< < 24 25 26 27 28 29 30 31 32 33 > >>
每頁顯示[10|25|50]項目
|
