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Showing items 436-460 of 594  (24 Page(s) Totally)
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Institution Date Title Author
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 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 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 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 Hydrops foetalis caused by anti-Mur in first pregnancy - a case report Wu, KH; Chang, JG; Lin, M; Shih, MC; Lin, HC; Lee, CC; Peng, CT; Tsai, CH
中國醫藥大學 2002 Hydrops foetalis caused by anti-Mur in first pregnancy - a case report Wu, KH; Chang, JG; Lin, M; Shih, MC; Lin, HC; Lee, CC; Peng, CT; Tsai, CH
中國醫藥大學 2002 Environmental risk factors of young onset Parkinson's disease: a case-control study Tsai, CH; Lo, SK; See, LC; Chen, HZ; Chen, RS; Weng, YH; Chang, FC; Lu, CS
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
中山醫學大學 2001 The correlation between alteration of p16 gene and clinical status in oral squamous cell carcinoma. Tsai, CH; Yang, CC; Chou, LS; Chou, MY
中山醫學大學 2001 The correlation between alteration of p16 gene and clinical status in oral squamous cell carcinoma. Tsai, CH; Yang, CC; Chou, LS; Chou, MY
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 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 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 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 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 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 Leukemia inhibitory factor decreases the arylamine N-acetyltransferase activity in human cumulus granulosa cells Chang, CC; Hsieh, YY; Chung, JG; Tsai, HD; Tsai, CH
中國醫藥大學 2001 Kinetics of acetyl coenzyme A: Arylamine N-acetyltransferase from human cumulus cells Chang, CC; Hsieh, YY; Chung, JG; Tsai, HD; Tsai, CH
中國醫藥大學 2001 Kinetics of acetyl coenzyme A: Arylamine N-acetyltransferase from human cumulus cells Chang, CC; Hsieh, YY; Chung, JG; 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 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

Showing items 436-460 of 594  (24 Page(s) Totally)
<< < 13 14 15 16 17 18 19 20 21 22 > >>
View [10|25|50] records per page