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显示项目 210591-210615 / 2348685 (共93948页)
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机构 日期 题名 作者
國立成功大學 2019-09 Association of the built environments and health-related quality of life in community-dwelling older adults: a cross-sectional study Huang;Nuan-Ching;Chu;Cordia;Kung;Shiann-Far;Hu;Susan, C.
國立成功大學 2019 Association of the built environments and health-related�quality of life in community-dwelling older adults: a cross-sectional study Huang, N.-C.;Chu, Chu C.;Kung, S.-F.;Hu, S.C.
中國醫藥大學 2011-01 Association of the C-285T and A5954G Polymorphisms in the DNA repair gene OGG1 with the Susceptibility of Rheumatoid Arthritis 陳世殷(Shih-Yin, Chen); 萬磊(Lei Wan); 黃春明(Chung-Ming Huang); 黃毓銓(Yu-Chuen Huang); 許晉銓(Jinn-Chyuan Sheu); 林應如(Ying-Ju Lin); 劉詩平(Shih-Ping Liu); 藍郁青(Yu-Ching Lan); 賴志和(Chih-HO Lai); 林振文(Lin Cheng Wen); 蔡長海(Chang-Hai Tsai); 蔡輔仁(Fuu-Jen Tsai)*
國立臺灣大學 2005-12 Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases Lee, CN; Su, YN; Cheng, WF; Lin, MT; Wang, JK; Wu, MH; Hsieh, FJ
國立臺灣大學 2005 ASSOCIATION OF THE C677T METHYLENETETRAHYDROFOLATE REDUCTASE MUTATION WITH CONGENITAL HEART DISEASES 李建南; 蘇怡寧; 鄭文芳; 林銘泰; 王主科; 吳美環; 李建南; 謝豐舟
臺大學術典藏 2020-02-06T05:22:29Z Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases Hsieh F.-J.;Wu M.-H.;Wang J.-K.;Lin M.-T.;WEN-FANG CHENG;Su Y.-N.;Lee C.-N.; Lee C.-N.; Su Y.-N.; WEN-FANG CHENG; Lin M.-T.; Wang J.-K.; Wu M.-H.; Hsieh F.-J.; Lee C.-N.; Su Y.-N.; WEN-FANG CHENG; Lin M.-T.; Wang J.-K.; Wu M.-H.; Hsieh F.-J.
臺大學術典藏 2020-02-12T04:06:26Z Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases Hsieh F.-J.;Wu M.-H;Wang J.-K;Lin M.-T;Cheng W.-F;Su Y.-N;CHIEN-NAN LEE; CHIEN-NAN LEE; Su Y.-N; Cheng W.-F; Lin M.-T; Wang J.-K; Wu M.-H; Hsieh F.-J.
臺大學術典藏 2020-02-14T02:50:12Z Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases Lee C.-N.;Su Y.-N.;Wen-Fang Cheng;Lin M.-T.;Wang J.-K.;Wu M.-H.;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; WEN-FANG CHENG; Lin M.-T.; Wang J.-K.; Wu M.-H.; Hsieh F.-J.
臺大學術典藏 2020-12-21T02:55:25Z Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases Lee C.-N.;Su Y.-N.;Cheng W.-F.;Ming-Tai Lin;Wang J.-K.;Wu M.-H.;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; Cheng W.-F.; MING-TAI LIN; Wang J.-K.; Wu M.-H.; Hsieh F.-J.
臺大學術典藏 2021-01-05T08:07:39Z Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases Lee C.-N.;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Wang J.-K.;Mei-Hwan Wu;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; Cheng W.-F.; Lin M.-T.; Wang J.-K.; MEI-HWAN WU; Hsieh F.-J.
臺大學術典藏 2021-01-06T05:46:48Z Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases Lee C.-N.;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Jou-Kou Wang;Wu M.-H.;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; Cheng W.-F.; Lin M.-T.; JOU-KOU WANG; Wu M.-H.; Hsieh F.-J.
臺大學術典藏 2021-02-04T06:05:12Z Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases Chien-Nan Lee;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Wang J.-K.;Wu M.-H.;Hsieh F.-J.; CHIEN-NAN LEE; Su Y.-N.; Cheng W.-F.; Lin M.-T.; Wang J.-K.; Wu M.-H.; Hsieh F.-J.
中國醫藥大學 2013-01 Association of the C825T polymorphism in the GNB3 gene with obesity and metabolic phenotypes in a Taiwanese population (Tun-Jen Hsiao);(Yuchi Hwang);(Can-Hong Liu);(Hua-Mei Chang);林詩鈞(Eugene Lin)*
國立臺灣大學 2012 Association of the Congenital Neuromuscular Form of Glycogen Storage Disease Type IV With a Large Deletion and Recurrent Frameshift Mutation Li, Sing-Chung; Hwu, Wuh-Liang; Lin, Ju-Li; Bali, Deeksha S.; Yang, Chen; Chu, Shih-Ming; Chien, Yin-Hsiu; Chou, Hung-Chieh; Chen, Chien-Yi; Hsieh, Wu-Shiun; Tsao, Po-Nien; Chen, Yuan-Tsong; Lee, Ni-Chung; 胡務亮; 謝武勳; 李妮鍾; 簡穎秀
臺大學術典藏 2020-12-09T01:38:32Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; Chen C.-Y.; Hsieh W.-S.; Tsao P.-N.; Chen Y.-T.; NI-CHUNG LEE
臺大學術典藏 2020-12-16T02:25:38Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Li S.-C.; WUH-LIANG HWU; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; Chen C.-Y.; Hsieh W.-S.; Tsao P.-N.; Chen Y.-T.; Lee N.-C.
臺大學術典藏 2020-12-22T03:29:29Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Lee N.-C.; Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; Chen C.-Y.; Hsieh W.-S.; PO-NIEN TSAO; Chen Y.-T.
臺大學術典藏 2020-12-24T02:03:54Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Lee N.-C.; Chen Y.-T.; Tsao P.-N.; Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; HUNG-CHIEH CHOU; Chen C.-Y.; Hsieh W.-S.
臺大學術典藏 2020-12-24T06:16:51Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Lee N.-C.; Chen Y.-T.; Tsao P.-N.; Hsieh W.-S.; Chen C.-Y.; Chou H.-C.; Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; YIN-HSIU CHIEN
臺大學術典藏 2021-01-21T02:05:00Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; CHIEN-YI CHEN; Hsieh W.-S.; Tsao P.-N.; Chen Y.-T.; Lee N.-C.
國立成功大學 2022 Association of the consumption of common drinks with early puberty in both sexes Tsai, M.-C.;Lee, Y.L.;Chen, Y.C.
國立成功大學 2024-01 Association of the Coronal Lateral Collateral Ligament Sign in ACL-Deficient Knees With Greater Anterior Tibial Translation and Femorotibial Rotation in Adults and Adolescents Lin;Yu-Ju;Cheng;Ting-An;Hsu;Kai-Lan;Kuan;Fa-Chuan;Su;Wei-Ren;Hong;Chih-Kai
中山醫學大學 2000 Association of the Cytoplasmic Membrane Protein XpsN with the Outer Membrane Protein XpsD in the Type II Protein Secretion Apparatus of Xanthomonas campestris pv. Campestris Lee, Hsien-Ming; Wang, Kuan-Cheng; Liu, Yi-Ling; Yew, Hsin-Yan; Chen, Ling-Yun; Leu, Wei-Ming; Chen, David Chanhen; Hu, Nien-Tai
國家衛生研究院 2022-01-04 Association of the D-amino acid oxidase gene with methadone dose in heroin dependent patients under methadone maintenance treatment Liu, TH;Tsou, HH;Chung, RH;Liu, SC;Wang, SC;Kuo, HW;Fang, CP;Chen, ACH;Liu, YL
輔英科技大學 2010-10-23 Association of the DNA Repair Gene hOGG1 Polymorphisms and Bladder Cancer Chih, Tsai-Tung;Chien, Shang-Tao;Lin, Su-Shuan ;Lin, Weng-Ling;Lin, Shih-Jung;Huang, Ching-Shan;Tang, Kung-Sheng

显示项目 210591-210615 / 2348685 (共93948页)
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