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Showing items 236-285 of 327 (7 Page(s) Totally)
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Institution	Date	Title	Author
中國醫藥大學	2002	Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學	2002	Turner syndrome with pseudodicentric Y chromosome mosaicism	Hsieh, YY; Lin, WC; Chang, CC; Tsai, FJ; Yu, MT; Tsai, HD; Tsai, CH
中國醫藥大學	2002	Turner syndrome with pseudodicentric Y chromosome mosaicism	Hsieh, YY; Lin, WC; Chang, CC; Tsai, FJ; Yu, MT; Tsai, HD; Tsai, CH
中國醫藥大學	2002	p21 gene codon 31 polymorphism is associated with bladder cancer	Chen, WC; Wu, HC; Hsu, CD; Chen, HY; Tsai, FJ
中國醫藥大學	2002	Relation of vitamin D receptor FokI start codon polymorphism. to bone mineral density and occurrence of osteoporosis in postmenopausal women in Taiwan	Chen, HY; Chen, WC; Hsu, CD; Tsai, FJ; Tsai, CH
中國醫藥大學	2002	Molecular analysis of thiopurine S-methyltransferase alleles in South-east Asian populations	Chang, JG; Lee, LS; Chen, CM; Shih, MC; Wu, MC; Tsai, FJ; Liang, DC
中國醫藥大學	2002	Unstable Hb Perth in a Taiwanese subject: A T -> C substitution at codon 32 of the beta-globin gene creates an MspI site	Chang, JG; Liu, HC; Shih, MC; Liu, SC; Chan, WL; Tsai, FJ
中國醫藥大學	2002	Unstable Hb Perth in a Taiwanese subject: A T -> C substitution at codon 32 of the beta-globin gene creates an MspI site	Chang, JG; Liu, HC; Shih, MC; Liu, SC; Chan, WL; 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	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	The voltage-gated potassium channel KCNQ2 in Taiwanese children with febrile convulsions	Chou, IC; Tsai, FJ; Huang, CC; Lin, CC; Tsai, CH
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	Prognostic significance of the proline form of p53 codon 72 polymorphism in nasopharyngeal carcinoma	Tsai, MH; Lin, CD; Hsieh, YY; Chang, FCC; Tsai, FJ; Chen, WC; Tsai, CH
中國醫藥大學	2002	Molecular analysis of thiopurine S-methyltransferase alleles in South-east Asian populations	Chang, JG; Lee, LS; Chen, CM; Shih, MC; Wu, MC; Tsai, FJ; Liang, DC
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	Distributions of p53 codon 72 polymorphism in primary open angle glaucoma	Lin, HJ; Chen, WC; Tsai, FJ; Tsai, SW
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	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	Calcitonin receptor gene polymorphism: A possible genetic marker for patients with calcium oxalate stones	Chen, WC; Wu, HC; Lu, HF; Chen, HY; Tsai, FJ
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	Hsieh, YY; Chang, CC; Tsai, FJ; Wu, JY; Shi, YR; Tsai, HD; Tsai, CH
中國醫藥大學	2001	p21 gene codon 31 arginine/serine polymorphism: Non-association with endometriosis	Hsieh, YY; Tsai, FJ; Chang, CC; Chen, WC; Tsai, CH; Tsai, HD; Lin, CC
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	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

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