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    Showing items 151-175 of 232. (10 Page(s) Totally)
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    DateTitleAuthors
    2001-12 Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation Wei-De Lin; Wu,Jer-Yuarn; Tsai,Fuu-Jen; Lee,Chun-Cheng; Chang-Hai Tsai
    2006-02 Mutation Analysis of Crouzon Syndrome in Taiwanese Patients Chin-Ping Chang; Lei Wan; Chang-Hai Tsai; Cheng-Chun Lee; Fuu-Jen Tsai
    2006-05 Mutation analysis of Gaucher disease patients in Taiwan: high prevalence of the RecNciI and L444P mutations Lei Wan; Hsu CM; Chang-Hai Tsai; Lee,Chun-Cheng; Hwu WL; Tsai,Fuu-Jen
    2006-06 Mutation analysis of Taiwanese Wilson disease patients Lei Wan; Chang-Hai Tsai; Yuhsin Tsai; Hsu CM; Lee,Chun-Cheng; Tsai,Fuu-Jen
    2002 Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan Shi YR; Wu,Jer-Yuarn; Hsu YA; Cheng-Chun Lee; Chang-Hai Tsai; Fuu-Jen Tsai
    2003 Neurodevelopment outcome of meconium aspiration syndrome at 2 years of age Lin Hung-Chih; Bai-Horng Su; Tsung-Wen Lin; Chang-Hai Tsai
    1996 Neuroimaging of pediatric cerebral infarctions Wu-Chung Shen; Chang-Hai Tsai; Su-Tso Yang
    2005 No association between TAP1 Dpn2 polymorphism and bronchopulmonary dysplasia Hung-Chih Lin; Bai-Horng Su; Chin-Moo Hsu; Kang-Hsi Wu; Hsiao-Chuan Lin; Fuu-Jen Tsai; Chang-Hai Tsai
    2005-09 No Association between TAP1 DpnII Polymorphism and Bronchopulmonary Dysplasia Hung-Chih Lin; Bai-Horng Su; Tsu-Fuh Yeh; Chang-Hai Tsai
    2004-07 No association of p53 codon 72 and p21 codon 31 polymorphisms in Taiwan Chinese patients with pterygium Yi-Yu Tsai; YW Cheng; Chiu-Yueh Lee; SH Tseng; Chang-Hai Tsai; Fuu-Jen Tsai
    2004-11 No association of urokinase gene 3'-UTR polymorphism with bronchopulmonary dysplasia for ventilated preterm infants Lin HC; Su BH; Lin TW; Hsu CM; Lei Wan; Chang-Hai Tsai; Fuu-Jen Tsai
    2005-10 No relationship between -627 interleukin-10 promoter polymorphism in Chinese patients with rheumatoid arthritis Chung-Ming Huang; Chang-Hai Tsai; Chi-Lan Chen; Chin-Ping Chang; Tsai,Fuu-Jen
    2000 Normal Values of Inner Canthal Distance, Interpupillary Distance and Palpebral Fissure Length in Normal Chinese Children in Taiwan Kang-Hsi Wu; Fuu-Jen Tsai; Tsai-Chung Li; Chang-Hai Tsai; Ching-Tien Peng; Tso-Ren Wang
    2009-10 A Novel Strategy for Designing Dual-target Inhibitors of KU86 and XRCC4 Chien-Yu Chen; Fuu-Jen Tsai; Jing-Gung Chung; Chang-Hai Tsai; Yuan-Man Hsu; Hung-Jin Huang; Tin-Yun Ho; Yea-Huey Chang; Da-Tian Bau; Ming-Hsui Tsai; Chen, Calvin Yu-Chian
    2005-03 Objective structured clinical examination (OSCE): A comparison of interpersonal skills scores with written part scores of OSCE 蘇百弘; 沈戊忠; 陳偉德; 洪瑞松; 蔡長海
    2004-03 Outcomes at School Age after Postnatal Dexamethasone Therapy for Lung Disease of Prematurity Tsu-Fuh Yeh; Yuh J. Lin; Lin Hung-Chih; Chao C. Huang; Wu S. Hsieh; CHIN-LIN CHANG; Chang-Hai Tsai
    2009-03 The p21 codon 31( *)C- and DRD2 codon 313( *)T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma Hsieh Yao-Yuan; Chang CC; Da-Tian Bau; Fuu-Jen Tsai; Tsai CH; Chen CP
    2001 p21 gene codon 31 arginine/serine polymorphism: Non-association with endometrosis Hsieh Yao-Yuan; Fuu-Jen Tsai; Chang CC; Chen Wen-Chi; Chang-Hai Tsai; Tsai HD; Cheng-Chieh Lin
    2008-03 p53 Codon 72 Proline/Arginine Polymorphism and Autoimmune Thyroid Diseases Rong-Hsing Chen; Chwen-Tzuei Chang; Tzu-Yuan Wang; Wen-Liang Huang; Chang-Hai Tsai; Fuu-Jen Tsai
    2006-11 Penil length of noormal boys in Taiwan Wei-De Lin; Chang-Hai Tsai; Da-Tian Bau; Tsai,Fuu-Jen
    2008-04 Pigment epithelium-derived factor gene Met72Thr polymorphism is associated with increased risk of wet age-related macular degeneration Lin Jane-Ming; Lei Wan; Yi-Yu Tsai; Hui-Ju Lin; Yuhsin Tsai; Cheng-Chun Lee; Chang-Hai Tsai; SUNG-HUEI TSENG; Fuu-Jen Tsai
    2001-07 A pilot study of neonatal screening by electrospray ionization tandem mass spectrometry in Taiwan Wei-De Lin; Wu,Jer-Yuarn; Lai,Chien-Chen; Tsai,Fuu-Jen; Chang-Hai Tsai
    2001-05 Pitfalls of PCR-based genotyping in patients with 21-hydroxylase deficiency Chang-Hai Tsai; Wei-De Lin; Tsai,Fuu-Jen; Peng,Ching-Tien; Wu,Jer-Yuarn
    2007-12 Polymorphism of XRCC1 Codon Arg 399 Gln Is Associated with Higher Susceptibility to Endometriosis Da-Tian Bau; Hsieh Yao-Yuan; Lei Wan; Rou-Fen Wang; Chiu-Chu Liao; Cheng-Chun Lee; Cheng-Chieh Lin; Chang-Hai Tsai; Fuu-Jen Tsai
    2002 Polymorphisms for interleukin 1 beta exon 5 and interleukin 1 receptor antagonist in Taiwanese children with febrile convulsions Fuu-Jen Tsai; Hsieh Yao-Yuan; Chi-Chen Chang; Cheng-Chieh Lin; Chang-Hai Tsai

    Showing items 151-175 of 232. (10 Page(s) Totally)
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