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Showing items 111-120 of 143 (15 Page(s) Totally)
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| 臺大學術典藏 |
2018-09-10T04:05:38Z |
Familial nephrogenic diabetes insipidus: report of two families.
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Lee, J.S.;Tsai, W.Y.;Tsai, W.S.;Tsau, Y.K.;Chen, C.H.;Wang, T.R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T04:05:21Z |
Familial nephrogenic diabetes insipidus: report of two families.
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Lee, J.S.;Tsai, W.Y.;Tsai, W.S.;Tsau, Y.K.;Chen, C.H.;Wang, T.R.; YONG-KWEI TSAU |
| 臺大學術典藏 |
2018-09-10T03:41:51Z |
Prader-Willi syndrome with chromosome 15 interstitial deletion: report of one case.
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Hwu, W.L.;Tsai, W.Y.;Lee, J.S.;Wang, P.J.;Wang, T.R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T03:32:25Z |
Wilson disease presenting as fulminant hepatic failure, acute hemolytic anemia and renal failure: report of one case
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Tseng, C.L.;Tsai, S.L.;Lin, K.H.;Chang, M.H.;Wang, T.R.;Hsu, Y.H.;Hsu, H.C.; KAI-HSIN LIN |
| 臺大學術典藏 |
2018-09-10T03:24:11Z |
Wiedemann-Beckwith syndrome with congenital central hypothyroidism in one of monozygotic twins.
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Chien, C.H.;Lee, J.S.;Tsai, W.Y.;Wang, T.R.; WEN-YU TSAI |
| 臺大學術典藏 |
1999 |
Molecular genetic study of Pompe disease in Chinese patients in Taiwan
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Ko T.-M.;Wuh-Liang Hwu;Lin Y.-W.;Tseng L.-H.;Hwa H.-L.;Wang T.-R.;Chuang S.-M.; Ko T.-M.; WUH-LIANG HWU; Lin Y.-W.; Tseng L.-H.; Hwa H.-L.; Wang T.-R.; Chuang S.-M. |
| 國立成功大學 |
1998-06 |
A curvature-ovalization measurement apparatus for circular tubes under cyclic bending
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Pan, Wen-Fung; Wang, T. R.; Hsu, C. M. |
| 臺大學術典藏 |
1998 |
Recommendations for management of severe enterovirus infection in Taiwan
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PING-ING LEE; Lee C.-Y.; Wang T.-R. |
| 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. |
| 臺大學術典藏 |
1996 |
Hepatoblastoma in an infant with Beckwith-Wiedemann Syndrome.
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Wang T.R.; Chang M.H.; YEN-HSUAN NI; Hwu W.L.; Jeng Y.M.; Tsai S.Y.;Jeng Y.M.;Hwu W.L.;Yen-Hsuan Ni;Chang M.H.;Wang T.R.; Tsai S.Y. |
Showing items 111-120 of 143 (15 Page(s) Totally)
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