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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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Institution Date Title Author
元智大學 2016-12-19 Novel Multiuser MIMO Relay Precoder Design for Cognitive Radio Systems with Primary Interference Cancellation Deng J.-H.; Su-Hua Chen
國立臺灣大學 2001 Novel Mutation in the Factor Vii Gene of Taiwanese Factor Vii-Deficient Patients 沈銘鏡; 林正修; 林淑華; 楊偉勛; 林博淂; SHEN, MING-CHING; LIN, JEN-SHIOU; LIN, SHU-WHA; YANG, WEI-SHIUNG; LIN, BO-DO
國立臺灣大學 2006-07 Novel mutation in the TSC2 gene associated with prenatally diagnosed cardiac rhabdomyomas and cerebral tuberous sclerosis Chen, CP; Su, YN; Hung, CC; Shih, JC; Wang, W
臺大學術典藏 2021-02-04T06:46:49Z Novel mutation in the TSC2 gene associated with prenatally diagnosed cardiac rhabdomyomas and cerebral tuberous sclerosis Chen C.-P.;Su Y.-N.;Hung C.-C.;Jin-Chung Shih;Wang W.; Chen C.-P.; Su Y.-N.; Hung C.-C.; JIN-CHUNG SHIH; Wang W.
國立成功大學 2022-09 Novel mutation of MAP3K1 gene in 46,XY DSD with complete gonadal dysgenesis Yu;Pei-Hsiu;Tsai;Meng-Che;Chiang;-Ting, Chun;Wang;Han-Yu;Kuo;Pao-Lin
國立臺灣大學 2006-07 Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal iscemic stroke Tang, SC; Lee, MJ; Jeng, JS; Yip, PK.
國立臺灣大學 2006 Novel Mutation of Neurofibromatosis Type 1 in a Patient with Cerebral Vasculopathy and Fatal Ischemic Stroke 湯頌君; 李銘仁; 鄭建興; 葉炳強; TANG, SUNG-CHUN; LEE, MING-JEN; JENG, JIANN-SHING; YIP, PING-KEUNG
國立臺灣大學 2006-06 NOVEL MUTATION OF NEUROFIBROMATOSIS TYPE 1 IN A PATIENT WITH CEREBRAL VASCULOPATHY AND FATAL ISCHEMIC STROKE 湯頌君; 李銘仁; 鄭建興; 葉炳強
臺大學術典藏 2020-03-04T05:35:24Z Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke SUNG-CHUN TANG;Yip P.-K.;Jeng J.-S;Lee M.-J; SUNG-CHUN TANG; Lee M.-J; Jeng J.-S; Yip P.-K.
臺大學術典藏 2020-03-02T12:11:30Z Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke SUNG-CHUN TANG;Yip P.-K.;Jeng J.-S;Lee M.-J; SUNG-CHUN TANG; Lee M.-J; Jeng J.-S; Yip P.-K.
臺大學術典藏 2018-09-10T05:46:48Z Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke Tang, S.-C. and Lee, M.-J. and Jeng, J.-S. and Yip, P.-K.; JIANN-SHING JENG; MING-JEN LEE; Sung-Chun Tang
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 2020-03-03T03:46:05Z 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.
臺大學術典藏 2020-03-04T05:43:05Z Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke SUNG-CHUN TANG; Lee M.-J; 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 Jeng J.-S.; Yip P.-K.; Lee M.-J.; SUNG-CHUN TANG; Sung-Chun Tang;Lee M.-J.;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 2006 Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke JIANN-SHING JENG; Yip P.-K.; Lee M.-J.; Tang S.-C.; Tang S.-C.;Lee M.-J.;Jiann-Shing Jeng;Yip P.-K.
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.

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