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機構 日期 題名 作者
中國醫藥大學 2000 G protein beta 3 subunit variant and essential hypertension in Taiwan - a case-control study Tsai, CH; Yeh, HI; Chou, YS; Liu, HF; Yang, TY; Wang, JC; Wang, NM; Chang, JG
中國醫藥大學 2000 Analysis of the mRNA transcripts of the survival motor neuron (SMN) gene in the tissue of an SMA fetus and the peripheral blood mononuclear cells of normals, carriers and SMA patients Jong, YJ; Chang, JG; Lin, SP; Yang, TY; Wang, JC; Chang, CP; Lee, CC; Li, H; Hsieh-Li, HM; Tsai, CH
中國醫藥大學 2000 Analysis of the mRNA transcripts of the survival motor neuron (SMN) gene in the tissue of an SMA fetus and the peripheral blood mononuclear cells of normals, carriers and SMA patients Jong, YJ; Chang, JG; Lin, SP; Yang, TY; Wang, JC; Chang, CP; Lee, CC; Li, H; Hsieh-Li, HM; Tsai, CH
中國醫藥大學 2000 Association of CTLA4 gene A-G polymorphism with type 1 diabetes in Chinese children Lee, YJ; Huang, FY; Lo, FS; Wang, WC; Hsu, CH; Kao, HA; Yang, TY; Chang, JG
中國醫藥大學 2000 G protein beta 3 subunit variant and essential hypertension in Taiwan - a case-control study Tsai, CH; Yeh, HI; Chou, YS; Liu, HF; Yang, TY; Wang, JC; Wang, NM; Chang, JG
中國醫藥大學 2000 Association of CTLA4 gene A-G polymorphism with type 1 diabetes in Chinese children Lee, YJ; Huang, FY; Lo, FS; Wang, WC; Hsu, CH; Kao, HA; Yang, TY; Chang, JG
中國醫藥大學 1999 Molecular characterization of secretor type alpha(1,2)-fucosyltransferase gene deficiency in the Philippine population Peng, CT; Tsai, CH; Lin, TP; Perng, LI; Kao, MC; Yang, TY; Wang, NM; Liu, TC; Lin, SF; Chang, JG
中國醫藥大學 1999 Molecular characterization of secretor type alpha(1,2)-fucosyltransferase gene deficiency in the Philippine population Peng, CT; Tsai, CH; Lin, TP; Perng, LI; Kao, MC; Yang, TY; Wang, NM; Liu, TC; Lin, SF; Chang, JG
中國醫藥大學 1999 Molecular analysis of secretor type alpha(1,2)-fucosyltransferase gene mutations in the Chinese and Thai populations Chang, JG; Yang, TY; Liu, TC; Lin, TP; Hu, CJ; Kao, MC; Wang, NM; Tsai, FJ; Peng, CT; Tsai, CH
中國醫藥大學 1999 Molecular analysis of secretor type alpha(1,2)-fucosyltransferase gene mutations in the Chinese and Thai populations Chang, JG; Yang, TY; Liu, TC; Lin, TP; Hu, CJ; Kao, MC; Wang, NM; Tsai, FJ; Peng, CT; Tsai, CH
中國醫藥大學 1999 Prenatal prediction of spinal muscular atrophy in Chinese Lin, SP; Chang, JG; Jong, YJ; Yang, TY; Tsai, CH; Wang, NM; Li, H; Hsieh-Li, HM; Hu, CJ
中國醫藥大學 1999 Hb Siriraj: a G -> A substitution at codon 7 of the beta-globin chain creates an MboII cutting site Chang, JG; Yang, TY; Perng, LI; Wang, NM; Peng, CT; Tsai, CH
中國醫藥大學 1999 Hb Siriraj: a G -> A substitution at codon 7 of the beta-globin chain creates an MboII cutting site Chang, JG; Yang, TY; Perng, LI; Wang, NM; Peng, CT; Tsai, CH
中國醫藥大學 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
中國醫藥大學 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
中國醫藥大學 1998.10 Human Rh Del is caused by a deletion of 1013 bp between introns 8 and 9 including exon 9 of Rh D gens 張建國(Chang JG*)*; (Wang JC); (Yang TY); (Tsan KW); 施木青(Mu-Chin Shih); 彭慶添(Ching-Tien Peng); 蔡長海(Chang-Hai Tsai)
亞洲大學 1998-10 Human Rh Del is caused by a deletion of 1013 bp between introns 8 and 9 including exon 9 of Rh D gens Chang JG;Wang JC;Yang TY;Tsan KW;Mu-Chin Shih;Ching-Tien Peng;Chang-Hai Tsai
中國醫藥大學 1998 Human RhDel IS caused by a deletion of 1,013 bp between introns 8 and 9 including exon 9 of RHD gene Chang, JG; Wang, JC; Yang, TY; Tsan, KW; Shih, MC
中國醫藥大學 1997 Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parents Chang, JG; Jong, YJ; Lin, SP; Soong, BW; Tsai, CH; Yang, TY; Chang, CP; Wang, WS

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