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Showing items 106-115 of 143 (15 Page(s) Totally)
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| 臺大學術典藏 |
2018-09-10T05:46:39Z |
Kleine-Levin syndrome in a boy with Prader-Willi syndrome
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Gau, S.-F.;Soong, W.-T.;Liu, H.-M.;Hou, J.-W.;Tsai, W.-Y.;Chiu, Y.-N.;Yeh, Y.-C.;Wang, P.-J.;Wang, T.-R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T05:46:28Z |
Camptomelic dysplasia: report of one case.
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Tsao, P.N.;Teng, R.J.;Hwu, W.L.;Tsou Yau, K.I.;Wang, T.R.; PO-NIEN TSAO |
| 臺大學術典藏 |
2018-09-10T05:12:25Z |
Prevalence of permanent primary congenital hypothyroidism in Taiwan.
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Tsai, W.Y.;Lee, J.S.;Chao, M.C.;Chen, L.Y.;Lin, S.J.;Wu, K.H.;Wang, T.R.;Chen, J.S.;Chuang, S.M.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T04:43:31Z |
Congenital nephrotic syndrome with microcephaly: report of a case.
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Yu, C.H.;Tsai, W.S.;Wang, P.J.;Tsau, Y.K.;Tseng, G.C.;Wang, T.R.; YONG-KWEI TSAU |
| 臺大學術典藏 |
2018-09-10T04:17:49Z |
DNA fingerprinting in the Chinese with an oligonucleotide probe (GTG)5.
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Hwu, W.L.;Chen, R.L.;Lin, K.H.;Wang, T.R.; KAI-HSIN LIN |
| 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 |
Showing items 106-115 of 143 (15 Page(s) Totally)
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