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"wu jy"
Showing items 226-235 of 257 (26 Page(s) Totally)
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| 中國醫藥大學 |
2001 |
Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele
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Hsieh, YY; Wu, JY; Chang, CC; Tsai, FJ; Lee, CC; Tsai, HD; Tsai, CH |
| 中國醫藥大學 |
2001 |
No association of vitamin D receptor gene BsmI polymorphisms with calcium oxalate stone formation
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Chen, WC; Chen, HY; Hsu, CD; Wu, JY; Tsai, FJ |
| 中國醫藥大學 |
2001 |
Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation
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Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH |
| 中國醫藥大學 |
2001 |
Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation
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Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH |
| 中國醫藥大學 |
2001 |
Mucopolysaccharidosis type VI: Report of two Taiwanese patients and identification of one novel mutation
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Yang, CF; Wu, JY; Lin, SP; Tsai, FJ |
| 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.
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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 |
Showing items 226-235 of 257 (26 Page(s) Totally)
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