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Showing items 281-305 of 327 (14 Page(s) Totally)
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| 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 |
Relation of the estrogen receptor alpha gene microsatellite polymorphism to bone mineral density and the susceptibility to osteoporosis in postmenopausal Chinese women in Taiwan
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Chen, HY; Chen, WC; Tsai, HD; Hsu, CD; Tsai, FJ; Tsai, CH |
| 中國醫藥大學 |
2001 |
Arginine form of p21 gene codon 31 is less prominent in patients with calcium oxalate stone
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Chen, WC; Lu, HF; Chen, HY; Hsu, CD; Tsai, FJ |
| 中國醫藥大學 |
2001 |
Lack of evidence for the association of tumor necrosis factor-alpha gene promoter polymorphism with calcium oxalate stone and bladder cancer patients
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Tsai, FJ; Lu, HF; Yeh, LS; Hsu, CD; Chen, WC |
| 中國醫藥大學 |
2001 |
Association of the vitamin D receptor gene start codon Fok I polymorphism with calcium oxalate stone disease
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Chen, WC; Chen, HY; Lu, HF; Hsu, CD; 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 |
Cytogenetic study of workers exposed to chromium compounds
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Wu, FY; Tsai, FJ; Kuo, HW; Tsai, CH; Wu, WY; Wang, RY; Lai, JS |
| 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 |
Infantile form G(M1) gangliosidosis with dilated cardiomyopathy: a case report
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Lin, HC; Tsai, FJ; Shen, WC; Tsai, CH; Peng, CT |
| 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 |
| 中國醫藥大學 |
2000 |
Antley-Bixler syndrome associated with Arnold-Chiari malformation
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Chang, YT; Tsai, FJ; Shen, WC; Lin, HC; Peng, CT; Tsai, CH |
| 中國醫藥大學 |
2000 |
Breech deformation complex in neonates
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Hsieh, YY; Tsai, FJ; Lin, CC; Chang, FCC; Tsai, CH |
| 中國醫藥大學 |
2000 |
Breech deformation complex in neonates
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Hsieh, YY; Tsai, FJ; Lin, CC; Chang, FCC; Tsai, CH |
| 中國醫藥大學 |
2000 |
Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency
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Lee, HH; Chang, JG; Tsai, CH; Tsai, FJ; Chao, HT; Chung, BC |
| 中國醫藥大學 |
2000 |
Mutation analysis of thyroid peroxidase gene in Taiwanese patients with total iodide organification defects: Identification of five novel mutations.
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Wu, J; Yang, CF; Tsai, FJ |
| 中國醫藥大學 |
2000 |
Aberrant transcripts of FHIT, TSG101 and PTEN/MMAC1 genes in normal peripheral mononuclear cells
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Wang, NM; Chang, JG; Liu, TC; Lin, SF; Peng, CT; Tsai, FJ; Tsai, CH |
| 中國醫藥大學 |
2000 |
Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency
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Lee, HH; Chang, JG; Tsai, CH; Tsai, FJ; Chao, HT; Chung, BC |
| 中國醫藥大學 |
1999 |
Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data
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Tsai, FJ; Tsai, CH; Chang, JG; Wu, JY |
| 中國醫藥大學 |
1999 |
Identification of a common N540K mutation in 8/18 Taiwanese hypochondroplasia patients: further evidence for genetic heterogeneity
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Tsai, FJ; Wu, JY; Tsai, CH; Chang, JG |
Showing items 281-305 of 327 (14 Page(s) Totally)
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