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"tsai fj"的相关文件
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| 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 |
| 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 |
| 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 |
1998 |
Mutation analysis in fibroblast growth factor receptor genes: Chinese data
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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
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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
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Peng, CT; Wu, JY; Tsai, CH; Tsai, FJ; Chang, JG |
| 中國醫藥大學 |
1998 |
Prenatal diagnosis of Apert syndrome
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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
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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
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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
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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
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Shen, WC; Tsai, FJ; Tsai, CH |
| 中國醫藥大學 |
1997 |
Mutations in fibroblast growth factor receptor genes: Chinese data.
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Tsai, FJ; Wu, JY; Peng, CT; Tsai, CH |
| 中國醫藥大學 |
1996 |
Catabolic effect in premature infants with early dexamethasone treatment
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Tsai, FJ; Tsai, CH; Wu, SF; Liu, YH; Yeh, TF |
| 中國醫藥大學 |
1996 |
Detection of congenital cytomegalovirus infection in Chinese newborn infants using polymerase chain reaction
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Tsai, CH; Tsai, FJ; Shih, YT; Wu, SF; Liu, SC; Tseng, YH |
| 中國醫藥大學 |
1996 |
X-linked recessive myotubular myopathy proven by muscle biopsy
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Tsai, CH; Huang, WS; Tsai, FJ; Lee, CC; Chen, SS |
| 中國醫藥大學 |
1996 |
X-linked recessive myotubular myopathy proven by muscle biopsy
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Tsai, CH; Huang, WS; Tsai, FJ; Lee, CC; Chen, SS |
| 中國醫藥大學 |
1993 |
MINOR ANOMALIES IN CHINESE NEWBORN-INFANTS
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TSAI, FJ; TSAI, CH |
| 中國醫藥大學 |
1992 |
NOMA NEONATORUM - AN UNUSUAL CASE OF NOMA INVOLVING A FULL-TERM NEONATE
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LIN, JY; WANG, DW; PENG, CT; TSAI, FJ; CHIOU, YM; TSAI, CH |
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