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教育部委托研究计画 计画执行:国立台湾大学图书馆
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"wu jy"的相关文件
显示项目 231-240 / 257 (共26页)
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| 中國醫藥大學 |
2001 |
Haplotype analysis in patients with velopharyngeal insufficiency (VPI) minimizes one VPI locus in 2.8Mb region of 22q11.
|
Tsai, LP; Tsou, KS; Shi, YR; Wu, JY; Tsai, FJ |
| 中國醫藥大學 |
2001 |
Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients
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Tsai, FJ; Yang, CF; Wu, JY; Tsai, CH; Lee, CC |
| 中國醫藥大學 |
2001 |
Interleukin-1 beta and interleukin-1 receptor antagonist gene polymorphisms in rheumatoid arthritis
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Huang, CM; Tsai, FJ; Wu, JY; Wu, MC |
| 中國醫藥大學 |
2000 |
Mutation analysis of type 2 Gaucher disease in Taiwan Chinese and identification of two novel mutations.
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Tsai, FJ; Wu, JY; Lin, SP; Chang, JG; Lee, CC; Tsai, CH |
| 中國醫藥大學 |
2000 |
Molecular analysis of syndromic congenital heart disease by using short tandem-repeat polymorphic markers.
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Shi, YR; Hsieh, KS; Wu, JY; Lee, CC; Tsai, CH; Tsai, FJ |
| 中國醫藥大學 |
2000 |
Molecular analysis of the N-acetylgalactosamina-6-sulfate sulfatase gene in Taiwanese patients with Mucopolysaccharidosis IVA.
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Yang, CF; Tsai, FJ; Lin, SP; Wu, JY |
| 中國醫藥大學 |
2000 |
Distributions of p53 codon 72 polymorphism in bladder cancer - proline form is prominent in invasive tumor
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Chen, WC; Tsai, FJ; Wu, JY; Wu, HC; Lu, HF; Li, CW |
| 中國醫藥大學 |
2000 |
A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia
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Tsai, FJ; Wu, JY; Lin, WD; Tsai, CH |
| 中國醫藥大學 |
2000 |
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) causes non-syndromic craniosynostosis
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Tsai, FJ; Wu, JY; Lee, CC; Tsai, CH |
| 義守大學 |
1999-07 |
Evaluation of intrinsic enantiomeric ratio by transient response method in a packed-bed enzymatic reactor
|
Wu JY |
显示项目 231-240 / 257 (共26页)
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