|
"stephenson d a"的相关文件
显示项目 11-20 / 20 (共1页)
1
每页显示[10|25|50]项目
| 臺大學術典藏 |
2020-03-03T02:33:34Z |
Recent developments in neurofibromatosis type 1
|
MING-JEN LEE; Stephenson D.A. |
| 臺大學術典藏 |
2020-03-03T02:33:33Z |
HMBS mutations in chinese patients with acute intermittent porphyria
|
Yang C.-C.; Kuo H.-C.; You H.-L.; Wang J.; Huang C.-C.; Liu C.-Y.; Lan M.-Y.; Stephenson D.A.; MING-JEN LEE |
| 臺大學術典藏 |
2020-03-03T02:33:29Z |
Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemia
|
MING-JEN LEE; Chien K.-L.; Chen M.-F.; Stephenson D.A.; Su T.-C. |
| 臺大學術典藏 |
2020-03-02T08:11:23Z |
Characterization of a familial case with primary erythromelalgia from Taiwan
|
Lee M.-J.;Yu H.-S.;Sung-Tsang Hsieh;Stephenson D.A.;Lu C.-J.;Yang C.-C.; Lee M.-J.; Yu H.-S.; SUNG-TSANG HSIEH; Stephenson D.A.; Lu C.-J.; Yang C.-C. |
| 臺大學術典藏 |
2018-09-10T06:50:20Z |
HMBS mutations in chinese patients with acute intermittent porphyria
|
Yang, C.-C.;Kuo, H.-C.;You, H.-L.;Wang, J.;Huang, C.-C.;Liu, C.-Y.;Lan, M.-Y.;Stephenson, D.A.;Lee, M.-J.; MING-JEN LEE; Chih-Chao Yang |
| 臺大學術典藏 |
2018-09-10T06:50:20Z |
Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum
|
李銘仁;鄭婷文;花茂棽;潘明楷;楊智超; Lee, M-J; Cheng, T-W; Hua, M-S; Pan, M-K; Wang, J; Stephenson, D A; Yang, C-C; Lee, M.-J. and Cheng, T.-W. and Hua, M.-S. and Pan, M.-K. and Wang, J. and Stephenson, D.A. and Yang, C.-C.; LEE, MING-JEN;CHENG, TING-WEN;HUA, MAU- SUN;PAN, MING-KAI;YANG, CHIH-CHAO; Lee, M-J; Ming-Kai Pan; MING-JEN LEE; Cheng, T-W; Chih-Chao Yang; Hua, M-S; Pan, M-K; Wang, J; LEE, MING-JEN; Stephenson, D A; Yang, C-C; CHENG, TING-WEN; HUA, MAU- SUN; PAN, MING-KAI; YANG, CHIH-CHAO |
| 臺大學術典藏 |
2018-09-10T06:40:07Z |
Characterization of a familial case with primary erythromelalgia from Taiwan
|
Lee, M.-J.;Yu, H.-S.;Hsieh, S.-T.;Stephenson, D.A.;Lu, C.-J.;Yang, C.-C.; SUNG-TSANG HSIEH; MING-JEN LEE; Chih-Chao Yang |
| 國立臺灣大學 |
2008 |
Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum
|
Lee, M-J; Cheng, T-W; Hua, M-S; Pan, M-K; Wang, J; Stephenson, D A; Yang, C-C |
| 國立臺灣大學 |
2008 |
Gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum
|
Yang, C. C., Lee, M. J., Tzen, K. Y., Cheng, T. W., Hua, M. S., Pan, M. R., Wang, J.; Stephenson, D. A. |
| 臺大學術典藏 |
2008 |
Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum
|
Lee M.-J.;Cheng T.-W.;Hua M.-S.;Ming-Kai Pan;Wang J.;Stephenson D.A.;Yang C.-C.; Lee M.-J.; Cheng T.-W.; Hua M.-S.; MING-KAI PAN; Wang J.; Stephenson D.A.; Yang C.-C. |
显示项目 11-20 / 20 (共1页)
1
每页显示[10|25|50]项目
|
