臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

關於TAIR
	計畫說明

瀏覽
	典藏機構
	作者
	題名
	日期
	統計圖表
	機構即時統計
	學術趨勢

消息
	2019臺灣學術機構典藏研討會
	機構典藏系統RC7版本已發佈

著作權
	出版社及期刊政策查詢
	TAIR著作權會議記錄

相關連結
	機構典藏計畫網站
	ROAR
	OpenDOAR
	SHERPA
	OAIster
	JAIRO
	Ira
	DSPACE
	RWWR
	臺大學術典藏NTU Scholars

跳至: [ 中文 ] [ 數字0-9 ] [ A B C D E F G H I J K L M N O P Q R S T U V W X Y Z ]

請輸入前幾個字:

顯示項目 621216-621225 / 2348570 (共234857頁)
<< < 62117 62118 62119 62120 62121 62122 62123 62124 62125 62126 > >>
每頁顯示[10|25|50]項目

機構	日期	題名	作者
臺大學術典藏	2020-03-03T02:33:35Z	Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke	Tang S.-C.; MING-JEN LEE; Jeng J.-S.; Yip P.-K.
臺大學術典藏	2006	Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke	Yip P.-K.; Jeng J.-S.; MING-JEN LEE; Tang S.-C.
臺大學術典藏	2021-12-22T03:54:38Z	Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke	Tang S.-C.; Lee M.-J.; JIANN-SHING JENG; Yip P.-K.
國家衛生研究院	2002-07-01	Novel mutation of topoisomerase I in rendering cells resistant to camptothecin	Chang, JY; Liu, JF; Juang, SH; Liu, TW; Chen, LT
中國醫藥大學	2002-07	Novel Mutation of Topoisomerase I in Rendering Cells Resistant to Camptothecin	(Chang, J.-Y.); (Liu, J.-F.); 莊聲宏(Shin-Hun Juang); (Liu T.-W.); (Chen, L.-T)
國立臺灣大學	1992	Novel Mutational Spectrum Induced by Nmethyl-NI-nitro-N-nitrosoguanidine in the Coding Region of the Hyposanthine (Guanine) Phosphoribosyltransferase Gene in Diploid Human Fibroblasts	Yang, J. L.; 吳成文; Yang, J. L.; Wu, Cheng-Wen
中山醫學大學	2006	Novel mutations at carboxyl terminus of CIC-1 channel in myotonia congenita	Kuo, H-C;Hsiao, K-M;Chang, L-I;You, T-H;Yeh, T-H;Huang, C-C
臺大學術典藏	2021-11-30T04:53:13Z	Novel mutations detection with next-generation sequencing and its association with clinical outcome in unilateral primary aldosteronism	Wu C.-H.; Peng K.-Y.; Hwang D.-Y.; Lin Y.-H.; VIN-CENT WU; Chueh J.S.
臺大學術典藏	2022-01-03T05:49:19Z	Novel mutations detection with next-generation sequencing and its association with clinical outcome in unilateral primary aldosteronism	Wu C.-H.; Peng K.-Y.; Hwang D.-Y.; Lin Y.-H.; Wu V.-C.; SHIH-CHIEH CHUEH
臺大學術典藏	2021-10-21T23:27:13Z	Novel mutations detection with next-generation sequencing and its association with clinical outcome in unilateral primary aldosteronism	Wu, Che Hsiung; Peng, Kang Yung; Hwang, Daw Yang; YEN-HUNG LIN; VIN-CENT WU; Chueh, Jeff S.

顯示項目 621216-621225 / 2348570 (共234857頁)
<< < 62117 62118 62119 62120 62121 62122 62123 62124 62125 62126 > >>
每頁顯示[10|25|50]項目

	English \| 正體中文 \| 简体中文 \| 總筆數 :0
	造訪人次 : 52547002 線上人數 : 993 教育部委託研究計畫計畫執行:國立臺灣大學圖書館