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机构 日期 题名 作者
國立交通大學 2014-12-08T15:27:52Z ARRANGING APPROPRIATE TRAINING ORDER IN NOISY DOMAINS HSU, YT; TSENG, SS; HONG, TP
亞洲大學 1994 Arranging appropriate training order in noisy domains Y. T. Hsu;S. S. Tseng;T. P. Hong
國立交通大學 2014-12-08T15:13:48Z Arranging numbers on circles to reach maximum total variations Liao, Ying-Jie; Shieh, Min-Zheng; Tsai, Shi-Chun
國立交通大學 2018-08-21T05:53:38Z Arranging silver nanowire arrays by microcontact printing for solar cells application Lin, Ching-Chang; Sun, Wen-Hsien; Liu, Shuenyu; Liu, Lai-Yi; Cheng, Chieh; Ko, Fu-Hsiang
國立臺灣科技大學 2018 Array Antenna Design and DSP Algorithm for 77 GHz FMCW Radars 段文順
亞洲大學 2014-02 Array CGH characterization of an unbalanced X-autosome translocation associated with Xq27.2-qter deletion, 11q24.3-qter duplication and Xq22.3-q27.1 duplication in a girl with primary amenorrhea and mental retardation 陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Kuo, Yu-Ling;Kuo, Yu-Ling;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yu-Ting;Chen, Yu-Ting;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen
亞洲大學 2014-02 Array CGH characterization of an unbalanced X-autosome translocation associated with Xq27.2-qter deletion, 11q24.3-qter duplication and Xq22.3-q27.1 duplication in a girl with primary amenorrhea and mental retardation Anonymous
亞洲大學 2018-10 Array comparative genomic hybridization characterization of a 3.3-Mb 17p13.3-p13.2 deletion encompassing YWHAE, CRK, HIC1 and PAFAH1B1 in an 8-year-old girl with Miller-Dieker lissencephaly syndrome, congenital heart defects, growth restriction and developmental delay 陳持平;Chen, Chih-Ping;Cha, Shu-Yuan;Chang, Shu-Yuan;Li, Shuan-Pei;Lin, Shuan-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen
臺大學術典藏 2020-02-12T04:05:43Z Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand-foot malformation. Role of EPS15L1 in pathogenesis Su Y.-N; Lin H.-Y; CHIEN-NAN LEE; Shih J.-C.; Hsueh Y.-L; Shih J.-C.;CHIEN-NAN LEE;Lin H.-Y;Su Y.-N;Hsueh Y.-L
臺大學術典藏 2021-02-04T06:46:33Z Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand-foot malformation. Role of EPS15L1 in pathogenesis Hsueh Y.-L.;Su Y.-N.;Lin H.-Y.;Lee C.-N.;Jin-Chung Shih; Hsueh Y.-L.; Su Y.-N.; Lin H.-Y.; Lee C.-N.; JIN-CHUNG SHIH

显示项目 203346-203355 / 2348973 (共234898页)
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每页显示[10|25|50]项目