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"wang t r"的相關文件
顯示項目 101-110 / 143 (共15頁)
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| 臺大學術典藏 |
2018-09-10T07:24:56Z |
Erratum: Molecular genetic study of Pompe disease in Chinese patients in Taiwan (Human Mutation (1999) 13 (380-384))
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Ko, T.-M.;Hwu, W.-L.;Lin, Y.-W.;Tseng, L.-H.;Hwa, H.-L.;Wang, T.-R.;Chuang S.-, M.;Hayashi, K.; LI-HUI TSENG; HSIAO-LIN HWA |
| 臺大學術典藏 |
2018-09-10T07:22:20Z |
Detection of KAL-1 gene deletion with fluorescence in situ hybridization
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Hou, J.-W.;Tsai, W.-Y.;Wang, T.-R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T06:14:53Z |
CATCH 22: Deletion of locus 22Q11 in velocardiofacial syndrome, digeorge anomaly, and nonsyndromic conotruncal defects
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Hou, J.-W.;Wang, J.-K.;Tsai, W.-Y.;Chou, C.-C.;Wang, T.-R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T06:14:53Z |
Partial DiGeorge anomaly associated with 10p deletion
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Hsu, H.-L.;Hsiao, P.-H.;Hou, J.-W.;Tsai, W.-Y.;Wang, T.-R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T06:06:32Z |
Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutation.
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Tsai, L.P.;Sue, W.C.;Hwu, W.L.;Lin, K.H.;Wang, T.R.; KAI-HSIN LIN |
| 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 |
顯示項目 101-110 / 143 (共15頁)
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