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Showing items 266-290 of 327  (14 Page(s) Totally)
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Institution Date Title Author
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 Antley-Bixler syndrome, description of two new cases and review of the literature Lee, HJ; Cho, DY; Tsai, FJ; Shen, WC
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 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 Interleukin-1 beta gene and receptor antagonist gene polymorphisms in patients with calcium oxalate stones Chen, WC; Wu, HC; Chen, HY; Wu, MC; Hsu, CD; Tsai, FJ
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

Showing items 266-290 of 327  (14 Page(s) Totally)
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