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Showing items 206-230 of 257 (11 Page(s) Totally)
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| 中國醫藥大學 |
2002 |
Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan
|
Shi, YR; Wu, JY; Hsu, YA; Lee, CC; Tsai, CH; Tsai, FJ |
| 中國醫藥大學 |
2002 |
Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan
|
Shi, YR; Wu, JY; Hsu, YA; Lee, CC; Tsai, CH; Tsai, FJ |
| 中國醫藥大學 |
2002 |
Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers
|
Lin, WD; Wu, JY; Tsai, FJ; Gau, MT; Lee, CC |
| 中國醫藥大學 |
2002 |
Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers
|
Lin, WD; Wu, JY; Tsai, FJ; Gau, MT; Lee, CC |
| 中國醫藥大學 |
2002 |
Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method
|
Shi, YR; Hsieh, KS; Wu, JY; Lee, CC; Tsai, CH; Tsai, FJ |
| 中國醫藥大學 |
2002 |
Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome
|
Wang, TJ; Huang, CB; Tsai, FJ; Wu, JY; Lai, RB; Hsiao, M |
| 中國醫藥大學 |
2002 |
Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome
|
Wang, TJ; Huang, CB; Tsai, FJ; Wu, JY; Lai, RB; Hsiao, M |
| 中國醫藥大學 |
2002 |
Association of vitamin D receptor gene BsmI polymorphisms in Chinese patients with systemic lupus erythematosus
|
Huang, CM; Wu, MC; Wu, JY; Tsai, FJ |
| 中國醫藥大學 |
2002 |
Lack of association of interleukin-1 beta gene polymorphisms in Chinese patients with systemic lupus erythematosus
|
Huang, CM; Wu, MC; Wu, JY; Tsai, FJ |
| 中國醫藥大學 |
2001 |
Androgen receptor trinucleotide polymorphism in endometriosis
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Hsieh, YY; Chang, CC; Tsai, FJ; Wu, JY; Tsai, CH; Tsai, HD |
| 中國醫藥大學 |
2001 |
Molecular analysis of GM1-gangliosidosis: identification and characterization of four novel mutations in two Taiwan Chinese patients.
|
Tsai, FJ; Yang, CF; Wu, JY |
| 中國醫藥大學 |
2001 |
Further evidence that fibroblast growth factor receptor 2 mutations cause Antley-Bixler syndrome
|
Tsai, FJ; Wu, JY; Yang, CF; Tsai, CH |
| 中國醫藥大學 |
2001 |
Molecular analysis of two patients with 3-hydroxy-methyl-glutaric aciduria: identification of three novel mutations including one de novo mutation.
|
Wu, JY; Yang, CF; Tsai, FJ |
| 中國醫藥大學 |
2001 |
Relation of polymorphism in the promotor region for the human osteocalcin gene to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan
|
Chen, HY; Tsai, HD; Chen, WC; Wu, JY; Tsai, FJ; Tsai, CH |
| 中國醫藥大學 |
2001 |
Polymorphisms for interleukin-1 beta (IL-1 beta)-511 promoter, IL-1 beta exon 5, and IL-1 receptor antagonist: Nonassociation with endometriosis
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Hsieh, YY; Chang, CC; Tsai, FJ; Wu, JY; Shi, YR; Tsai, HD; Tsai, CH |
| 中國醫藥大學 |
2001 |
Osteocalcin gene Hind III polymorphism is not correlated with calcium oxalate stone disease
|
Chen, WC; Chen, HY; Wu, JY; Chen, YT; Tsai, FJ |
| 中國醫藥大學 |
2001 |
Osteocalcin gene Hind III polymorphism is not correlated with calcium oxalate stone disease
|
Chen, WC; Chen, HY; Wu, JY; Chen, YT; 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
|
Huang, CM; Tsai, FJ; Wu, JY; Wu, MC |
| 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 |
Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele
|
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
|
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
|
Yang, CF; Wu, JY; Lin, SP; Tsai, FJ |
Showing items 206-230 of 257 (11 Page(s) Totally)
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