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Showing items 36-37 of 37 (1 Page(s) Totally) 1 View [10|25|50] records per page
| 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. |
Showing items 36-37 of 37 (1 Page(s) Totally) 1 View [10|25|50] records per page
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