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教育部委託研究計畫 計畫執行:國立臺灣大學圖書館
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顯示項目 603176-603185 / 2348419 (共234842頁)
<< < 60313 60314 60315 60316 60317 60318 60319 60320 60321 60322 > >>
每頁顯示[10|25|50]項目
| 中國醫藥大學 |
2003 |
Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency
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Lee, HH; Chang, SF; Tsai, FJ; Tsai, LP; Lin, CY |
| 中國醫藥大學 |
2003.06 |
Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency.
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(Lee HH); (Chang SF); 蔡輔仁(Fuu-Jen Tsai); (Tsai LP); (Lin CY) |
| 中國醫藥大學 |
2003.06 |
Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency.
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(Lee HH); (Chang SF); 蔡輔仁(Fuu-Jen Tsai); (Tsai LP); (Lin CY) |
| 臺北醫學大學 |
2003 |
Mutation of IVS2-12A/C>G together with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency
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張淑芬; Hsien-Hsiung Lee; Shwu-Fen Chang; Fuu-Jen Tsai; Li-Ping Tsai; Ching-Yu Lin |
| 臺大學術典藏 |
2018-09-10T06:41:55Z |
Mutation of keratin 9 (R163W) in a family with epidermolytic palmoplantar keratoderma and knuckle pads
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Sheen, Y.-S.;Chu, C.-Y.;Lin, P.-J.;Liaw, S.-H.;Chiu, H.-C.;Jee, S.-H.; HSIEN-CHING CHIU; SHIOU-HWA JEE; CHIA-YU CHU; Yi-Shuan Sheen |
| 臺大學術典藏 |
2019-12-04T08:44:13Z |
Mutation of keratin 9 (R163W) in a family with epidermolytic palmoplantar keratoderma and knuckle pads
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Sheen Y.-S.;Chia-Yu Chu;Lin P.-J.;Liaw S.-H.;Chiu H.-C.;Jee S.-H.; Sheen Y.-S.; CHIA-YU CHU; Lin P.-J.; Liaw S.-H.; Chiu H.-C.; Jee S.-H. |
| 臺大學術典藏 |
2019-12-05T06:26:50Z |
Mutation of keratin 9 (R163W) in a family with epidermolytic palmoplantar keratoderma and knuckle pads
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Sheen Y.-S.;Chu C.-Y.;Lin P.-J.;Liaw S.-H.;Hsien-Ching Chiu;Jee S.-H.; Sheen Y.-S.; Chu C.-Y.; Lin P.-J.; Liaw S.-H.; HSIEN-CHING CHIU; Jee S.-H. |
| 國立臺灣大學 |
2007-01 |
Mutation of keratin 9 (R163W) in a family with epidermolytic palmoplantar keratoderma and knuckle pads.
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Sheen, YS; Chu, CY; Lin, PJ; Liaw, SH; Chiu, HC; Jee, SH |
| 慈濟大學 |
1996 |
Mutation of Lysines in a Plasminogen Binding Region of Streptokinase Identifies Residues Important for Generating a Functional Activator Complex
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Lin, Lee-Fong;Oeun, Saravuth;Houng, Aiilyan;Reed, Guy L. |
| 臺大學術典藏 |
2008 |
Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy
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Wang S.-B.; Weng W.-C.; Lee N.-C.; Hwu W.-L.; PI-CHUAN FAN; Lee W.-T. |
顯示項目 603176-603185 / 2348419 (共234842頁)
<< < 60313 60314 60315 60316 60317 60318 60319 60320 60321 60322 > >>
每頁顯示[10|25|50]項目
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