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    顯示項目2626-2650 / 5608. (共225頁)
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    日期題名作者
    2009-11-11 Muscarinic acetylcholine receptor 1 gene polymorphisms associated with high myopia. 邱育德(Yu-Te Chiu); 崔永平(Yung-Ping Tsui); 林慧茹(Hui-Ju Lin)
    2007-03 The Mustard-Restelli(double switch) procedure for anatomical repair of congenitally corrected transposition of the great arteries 黃懷緒(Huai-Hsu Huang); 李明禮(Ming-Li Li); 丁志中(Chih-Chung Ting); 李秉純(Ping-Chun Li)
    1998 Mutation analysis in fibroblast growth factor receptor genes: Chinese data Lin, SP; Tsai, FJ; Wu, JY; Peng, CT; Tsai, CH
    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
    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
    2000 Mutation analysis of BCL 10 in acute myeloid leukaemia Liu, TC; Lin, PM; Chang, JG; Lee, JP; Chen, TP; Sue, YC; Lin, SF
    1998 Mutation analysis of Chinese patients with Wilson disease Tsai, FJ; Wu, JY; Chang, JG; Lin, SP; Peng, CT; Tsai, CH
    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
    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
    2003 Mutation analysis of CTNNB1 (beta-catenin) and AXINI, the components of Wnt pathway, in cervical carcinomas Su, TH; Chang, JG; Yeh, KT; Lin, TH; Lee, TP; Chen, JC; Lin, CC
    2003 Mutation analysis of CTNNB1 (beta-catenin) and AXINI, the components of Wnt pathway, in cervical carcinomas Su, TH; Chang, JG; Yeh, KT; Lin, TH; Lee, TP; Chen, JC; Lin, CC
    2000 Mutation analysis of PTEN/MMAC1 in acute myeloid leukemia Liu, TC; Lin, PM; Chang, JG; Lee, JP; Chen, TP; Lin, SF
    2000 Mutation analysis of PTEN/MMAC1 in acute myeloid leukemia Liu, TC; Lin, PM; Chang, JG; Lee, JP; Chen, TP; Lin, SF
    2002 Mutation analysis of the EXT genes in Taiwanese patients with hereditary multiple exostoses Tsai, F; Shi, Y; Wu, J; Tsai, C
    1999 Mutation analysis of the PTEN/MMAC1 gene in cancers of the digestive tract Chang, JG; Chen, YJ; Perng, LI; Wang, NM; Kao, MC; Yang, TY; Chang, CP; Tsai, CH
    1999 Mutation analysis of the PTEN/MMAC1 gene in cancers of the digestive tract Chang, JG; Chen, YJ; Perng, LI; Wang, NM; Kao, MC; Yang, TY; Chang, CP; Tsai, CH
    1999 Mutation analysis of the putative tumor suppression gene PTEN/MMAC1 in sporadic breast cancer Chen, ST; Yu, SY; Tsai, M; Yeh, KT; Wang, JC; Kao, MC; Shih, MC; Chang, JG
    1999 Mutation analysis of the putative tumor suppression gene PTEN/MMAC1 in sporadic breast cancer Chen, ST; Yu, SY; Tsai, M; Yeh, KT; Wang, JC; Kao, MC; Shih, MC; Chang, JG
    2000 Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in cervical cancer Su, TH; Chang, JG; Perng, LI; Chang, CP; Wei, HJ; Wang, NM; Tsai, CH
    2000 Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in cervical cancer Su, TH; Chang, JG; Perng, LI; Chang, CP; Wei, HJ; Wang, NM; Tsai, CH
    2000 Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in hepatocellular carcinoma Yeh, KT; Chang, JG; Chen, YJ; Chen, ST; Yu, SY; Shih, MC; Perng, LI; Wang, JC; Tsai, M; Chang, CP
    2000 Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in hepatocellular carcinoma Yeh, KT; Chang, JG; Chen, YJ; Chen, ST; Yu, SY; Shih, MC; Perng, LI; Wang, JC; Tsai, M; Chang, CP
    2002 Mutation analysis of thyroid peroxidase gene in Chinese patients with total iodide organification defect: Identification of five novel mutations Wu, JY; Shu, SG; Yang, CF; Lee, CC; Tsai, FJ
    2000 Mutation analysis of thyroid peroxidase gene in Taiwanese patients with total iodide organification defects: Identification of five novel mutations. Wu, J; Yang, CF; Tsai, FJ
    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

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