| 臺大學術典藏 |
2018-09-10T04:24:41Z |
Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deagness
|
Hwa, H.-L. and Ko, T.-M. and Hsu, C.-J. and Huang, C.-H. and Chiang, Y.-L. and Oong, J.-L. and Chen, C.-C. and Hsu, C.-K.; HSIAO-LIN HWA |
| 臺大學術典藏 |
2020-02-03T08:15:24Z |
Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deagness
|
Hsiao-Lin Hwa;Ko T.-M.;Hsu C.-J.;Huang C.-H.;Chiang Y.-L.;Oong J.-L.;Chen C.-C.;Hsu C.-K.; HSIAO-LIN HWA; Ko T.-M.; Hsu C.-J.; Huang C.-H.; Chiang Y.-L.; Oong J.-L.; Chen C.-C.; Hsu C.-K. |
| 國立臺灣大學 |
2009 |
Mutation Spectrum of the Fibrillin-1 (Fbn1) Gene in Taiwanese Patients with Marfan Syndrome
|
洪加政; 李建南; 鄭惠予; 林炫沛; 陳銘仁; 陳持平; 張千慧; 游治節; 邱馨慧; 鄭文芳; 何弘能; 牛道明; 蘇怡寧; HUNG, CHIA-CHENG; LEE, CHIEN-NAN; CHENG, HUI-YU; LIN, SHUAN-PEI; CHEN, MING-REN; CHEN, CHIH-PING; CHANG, CHIEN-HUI; YU, CHIH- CHIEH; CHIU, HSIN-HUI; CHENG, WEN-FANG; HO, HONG-NERNG; NIU, DAU-MING; SU, YI-NING |
| 臺大學術典藏 |
2018-09-10T07:23:46Z |
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
|
Hung, C.-C. and Lin, S.-Y. and Lee, C.-N. and Cheng, H.-Y. and Lin, S.-P. and Chen, M.-R. and Chen, C.-P. and Chang, C.-H. and Lin, C.-Y. and Yu, C.-C. and Chiu, H.-H. and Cheng, W.-F. and Ho, H.-N. and Niu, D.-M. and Su, Y.; SHIN-YU LIN; HONG-NERNG HO; WEN-FANG CHENG; CHIH-CHIEH YU; CHIEN-NAN LEE |
| 臺大學術典藏 |
2020-02-06T05:22:16Z |
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
|
Chen C.-P.; Chang C.-H.; Lin C.-Y.; Yu C.-C.; Chiu H.-H.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.; Chen M.-R.; Lin S.-P.; Cheng H.-Y.; Su Y.;Niu D.-M.;Ho H.-N.;WEN-FANG CHENG;Chiu H.-H.;Yu C.-C.;Lin C.-Y.;Chang C.-H.;Chen C.-P.;Chen M.-R.;Lin S.-P.;Cheng H.-Y.;Lee C.-N.;Lin S.-Y.;Hung C.-C.; Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin S.-P.; Chen M.-R.; Chen C.-P.; Chang C.-H.; Lin C.-Y.; Yu C.-C.; Chiu H.-H.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.; Hung C.-C.; Lin S.-Y.; Lee C.-N. |
| 臺大學術典藏 |
2009 |
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
|
Su Y.;Niu D.-M;Ho H.-N;Cheng W.-F;Chiu H.-H;Yu C.-C;Lin C.-Y;Chang C.-H;Chen C.-P;Chen M.-R;Lin S.-P;Cheng H.-Y;CHIEN-NAN LEE;Lin S.-Y;Hung C.-C; Hung C.-C; Lin S.-Y; CHIEN-NAN LEE; Cheng H.-Y; Lin S.-P; Chen M.-R; Chen C.-P; Chang C.-H; Lin C.-Y; Yu C.-C; Chiu H.-H; Cheng W.-F; Ho H.-N; Niu D.-M; Su Y. |
| 臺大學術典藏 |
2020-02-14T02:50:02Z |
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
|
Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin S.-P.; Chen M.-R.; Chen C.-P.; Chang C.-H.; Lin C.-Y.; Yu C.-C.; Chiu H.-H.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y. |
| 臺大學術典藏 |
2020-02-17T07:43:41Z |
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
|
Hung C.-C; Lin S.-Y; Lee C.-N; Cheng H.-Y; Lin S.-P; Chen M.-R; Chen C.-P; Chang C.-H; Lin C.-Y; Yu C.-C; Chiu H.-H; Cheng W.-F; HONG-NERNG HO; Niu D.-M; Su Y. |
| 臺大學術典藏 |
2020-12-28T10:02:47Z |
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
|
Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin S.-P.; Chen M.-R.; Chen C.-P.; Chang C.-H.; Lin C.-Y.; CHIH-CHIEH YU; Chiu H.-H.; Cheng W.-F.; Ho H.-N.; Niu D.-M.; Su Y. |
| 臺大學術典藏 |
2021-09-09T07:52:50Z |
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
|
Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin S.-P.; Chen M.-R.; Chen C.-P.; Chang C.-H.; Lin C.-Y.; CHIH-CHIEH YU; Chiu H.-H.; Cheng W.-F.; Ho H.-N.; Niu D.-M.; Su Y. |
| 臺大學術典藏 |
2022-09-19T07:17:43Z |
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
|
Hung, Chia-Cheng; Lin, Shin-Yu; Lee, Chien-Nan; Cheng, Hui-Yu; Lin, Shuan-Pei; Chen, Ming-Ren; Chen, Chih-Ping; Chang, Chien-Hui; Lin, Chiou-Ya; CHIH-CHIEH YU; Chiu, Hsin-Hui; Cheng, Wen-Fang; Ho, Hong-Nerng; Niu, Dau-Ming; Su, Yi-Ning |
| 國立臺灣大學 |
2016 |
Mutation-adapted U1 snRNA corrects a splicing error of the dopa decarboxylase gene
|
Lee, Ni-Chung; Lee, Yu-May; Chen, Pin-Wen; Byrne, Barry J.; Hwu, Wuh-Liang; 胡務亮; 李妮鍾 |
| 臺大學術典藏 |
2016 |
Mutation-adapted U1 snRNA corrects a splicing error of the dopa decarboxylase gene
|
NI-CHUNG LEE; Lee Y.-M.; Chen P.-W.; Byrne B.J.; Hwu W.-L. |
| 臺大學術典藏 |
2020-12-16T02:25:21Z |
Mutation-adapted U1 snRNA corrects a splicing error of the dopa decarboxylase gene
|
Lee N.-C.; Lee Y.-M.; Chen P.-W.; Byrne B.J.; WUH-LIANG HWU |
| 臺大學術典藏 |
2020-03-05T01:18:03Z |
Mutational analysis of Angiogenin gene in Parkinson's disease
|
Chen M.-L.; Wu R.-M.; CHUN-HWEI TAI; Lin C.-H. |
| 臺大學術典藏 |
2020-03-04T07:45:29Z |
Mutational analysis of Angiogenin gene in Parkinson's disease
|
Chen M.-L.; Wu R.-M.; Tai C.-H.; CHIN-HSIEN LIN |
| 臺大學術典藏 |
2018-09-10T14:55:30Z |
Mutational analysis of Angiogenin gene in Parkinson's disease
|
Chen, M.-L. and Wu, R.-M. and Tai, C.-H. and Lin, C.-H.; Chin-Hsien Lin |
| 臺大學術典藏 |
2020-02-25T08:01:23Z |
Mutational analysis of Angiogenin gene in Parkinson's disease
|
Chen M.-L; RUEY-MEEI WU; Tai C.-H; Lin C.-H. |
| 臺大學術典藏 |
2020-11-03T12:12:48Z |
Mutational analysis of Angiogenin gene in Parkinson's disease
|
Chen M.-L.; Wu R.-M.; Tai C.-H.; CHIN-HSIEN LIN |
| 臺大學術典藏 |
2020-11-03T12:21:50Z |
Mutational analysis of Angiogenin gene in Parkinson's disease
|
Lin C.-H.; CHUN-HWEI TAI; Wu R.-M.; Chen M.-L. |
| 國立臺灣大學 |
1994 |
Mutational Analysis of Delta Antigen: Effect on Assembly and Replication of Hepatitis Delta Virus
|
張明富; 陳春榮; 張鑫; CHANG, MING-FU; CHEN, CHUN-JUNG; CHANG, SHIN-C. |
| 臺大學術典藏 |
2019-08-30T02:32:35Z |
Mutational analysis of delta antigen: Effect on assembly and replication of hepatitis delta virus
|
Ming-Fu Chang;Chen C.-J.;Chang, S.C.; MING-FU CHANG; Chen C.-J.; Chang, S.C. |
| 臺大學術典藏 |
2019-11-11T08:48:47Z |
Mutational analysis of delta antigen: Effect on assembly and replication of hepatitis delta virus
|
Ming-Fu Chang;Chen C.-J.;Chang S.C.; MING-FU CHANG; Chen C.-J.; Chang S.C. |
| 國立成功大學 |
2022-12-28 |
Mutational analysis of epidermolysis bullosa in Taiwan by whole-exome sequencing complemented by RNA sequencing: a series of 77 patients
|
Tu;Wei-Ting;Hou;Ping-Chen;Chen;Peng-Chieh;Chen;Wan-Rung;Huang;Hsin-Yu;Wang;Jing-Yu;Huang;Yi-Ting;Wu;Yi-Huei;Su;Chun-Lin;Tang;Yen-An;Iwata;Hiroaki;Natsuga;Ken;Chao;Sheau-Chiou;Sun;Sunny, H.;Tang;Ming-Jer;Lee;Julia, Yu-Yun;McGrath;John, A. A.;Hsu;Chao-Kai |
| 國立成功大學 |
2022-12 |
Mutational analysis of epidermolysis bullosa in Taiwan by whole-exome sequencing complemented by RNA sequencing: a series of 77 patients.
|
Tu, Wei-Ting;Hou, Ping-Chen;Chen, Peng-Chieh;Chen, Wan-Rung;Huang, Hsin-Yu;Wang, Jing-Yu;Huang, Yi-Ting;Wu, Yi-Huei;Su, Chun-Lin;Tang, Yen-An;Iwata, Hiroaki;Natsuga, Ken;Chao, Sheau-Chiou;Sun, H. Sunny;Tang, Ming-Jer;Lee, Julia Yu-Yun;McGrath, John A.;Hsu, Chao-Kai; HSU, CHAO-KAI; 許釗凱 |
