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Showing items 81-94 of 94 (4 Page(s) Totally)
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| 中國醫藥大學 |
2000 |
Association of CTLA4 gene A-G polymorphism with type 1 diabetes in Chinese children
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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Chang, JG; Jong, YJ; Lin, SP; Soong, BW; Tsai, CH; Yang, TY; Chang, CP; Wang, WS |
Showing items 81-94 of 94 (4 Page(s) Totally)
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