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Showing items 621951-621960 of 2351427 (235143 Page(s) Totally)
<< < 62191 62192 62193 62194 62195 62196 62197 62198 62199 62200 > >>
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| 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. |
| 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. |
| 國立臺灣師範大學 |
2014-10-27T15:01:12Z |
Novel Mutations in c-Cb1 Ubiquitin Ligase Gene in Taiwanese Lung Cancer
|
譚一泓; Salgia, Ravi; 謝秀梅; 王憶卿 |
| 中山醫學大學 |
2010 |
Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss
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Hui-Mei Hong; Jiann-Jou Yang; Jia-Ching Shieh; Mei-Ling Li; Shuan-Yow Li |
Showing items 621951-621960 of 2351427 (235143 Page(s) Totally)
<< < 62191 62192 62193 62194 62195 62196 62197 62198 62199 62200 > >>
View [10|25|50] records per page
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