|
"tsai fj"的相關文件
顯示項目 311-320 / 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 |
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 |
顯示項目 311-320 / 327 (共33頁)
<< < 24 25 26 27 28 29 30 31 32 33 > >>
每頁顯示[10|25|50]項目
|
