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机构 日期 题名 作者
中國醫藥大學 2001 Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots Lai, CC; Tsai, CH; Tsai, FJ; Lee, CC; Lin, WD
中國醫藥大學 2001 Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots Lai, CC; Tsai, CH; Tsai, FJ; Lee, CC; Lin, WD
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 The association of androgen- and oestrogen-receptor gene polymorphisms with urolithiasis in men Chen, WC; Wu, HC; Lin, WC; Wu, MC; Hsu, CD; Tsai, FJ
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 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 Relation of BsmI vitamin D receptor gene polymorphism to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan Chen, HY; Chen, WC; Hsu, CD; Tsai, FJ; Tsai, CH; Li, CW
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 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 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
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 Relation of the estrogen receptor alpha gene microsatellite polymorphism to bone mineral density and the susceptibility to osteoporosis in postmenopausal Chinese women in Taiwan 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 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 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 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 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 2000 Mutation analysis of type 2 Gaucher disease in Taiwan Chinese and identification of two novel mutations. 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. 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. Yang, CF; Tsai, FJ; Lin, SP; Wu, JY
中國醫藥大學 2000 Cytogenetic study of workers exposed to chromium compounds 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 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 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 Lin, HC; Tsai, FJ; Shen, WC; Tsai, CH; Peng, CT

显示项目 271-295 / 327 (共14页)
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