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"tsai l p"的相关文件
显示项目 31-37 / 37 (共4页)
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| 臺大學術典藏 |
2018 |
Functional independence of Taiwanese children with Prader–Willi syndrome
|
Lee C.-L.;Lin H.-Y.;Tsai L.-P.;Chiu H.-C.;Tu R.-Y.;Huang Y.-H.;Chien Y.-H.;Ni-Chung Lee;Niu D.-M.;Chao M.-C.;Tsai F.-J.;Chou Y.-Y.;Chuang C.-K.;Lin S.-P.; Lee C.-L.; Lin H.-Y.; Tsai L.-P.; Chiu H.-C.; Tu R.-Y.; Huang Y.-H.; Chien Y.-H.; NI-CHUNG LEE; Niu D.-M.; Chao M.-C.; Tsai F.-J.; Chou Y.-Y.; Chuang C.-K.; Lin S.-P. |
| 國立成功大學 |
2018 |
Functional independence of Taiwanese children with Prader–Willi syndrome
|
Lee, C.-L.;Lin, H.-Y.;Tsai, L.-P.;Chiu, H.-C.;Tu, R.-Y.;Huang, Y.-H.;Chien, Y.-H.;Lee, N.-C.;Niu, D.-M.;Chao, M.-C.;Tsai, F.-J.;Chou, Y.-Y.;Chuang, Chuang C.-K.;Lin, S.-P. |
| 臺大學術典藏 |
2012 |
A novel 3670-base pair mitochondrial DNA deletion resulting in multi-systemic manifestations in a child
|
Lee N.-C.; Hwu W.-L.; Tsai I.-J.; Lee W.-T.; Huang P.-H.; Wu E.-T.; Weng W.-C.; Peng S.-F.; Chien Y.-H.; Wu J.-F.; Tsai L.-P.; Liu H.-M. |
| 臺大學術典藏 |
2012 |
A novel 3670-base pair mitochondrial DNA deletion resulting in multi-systemic manifestations in a child
|
Liu H.-M.; Tsai L.-P.; YIN-HSIU CHIEN; Wu J.-F.; Weng W.-C.; Peng S.-F.; Wu E.-T.; Huang P.-H.; Lee W.-T.; Tsai I.-J.; Hwu W.-L.; Lee N.-C. |
| 臺大學術典藏 |
2012 |
A novel 3670-base pair mitochondrial DNA deletion resulting in multi-systemic manifestations in a child
|
Huang P.-H.; Wu E.-T.; Peng S.-F.; WEN-CHIN WENG; Wu J.-F.; Chien Y.-H.; Tsai L.-P.; Liu H.-M.; Lee W.-T.; Tsai I.-J.; Hwu W.-L.; Lee N.-C. |
| 臺大學術典藏 |
1996 |
Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutation.
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Tsai L.P.;Sue W.C.;Wuh-Liang Hwu;Lin K.H.;Wang T.R.; Tsai L.P.; Sue W.C.; WUH-LIANG HWU; Lin K.H.; Wang T.R. |
| 國立臺灣大學 |
1995 |
Glucose-6-phosphate Gene G327 is a Common Mutation in Chinese Patients with Glycogen Storage Disease Type I
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胡務亮; Wang, W. C.; Cheng, J. R.; Chuang, S. C.; Tsai, L. P.; Wang, T. R.; Hwu, Wuh-Liang; Wang, W. C.; Cheng, J. R.; Chuang, S. C.; Tsai, L. P.; Wang, T. R. |
显示项目 31-37 / 37 (共4页)
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