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Showing items 1-4 of 4 (1 Page(s) Totally)
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| 臺大學術典藏 |
2018-09-10T07:02:24Z |
A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: Possible correlation with poor response to fetal therapy
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Ma, G.-C.;Liu, C.-S.;Chang, S.-P.;Yeh, K.-T.;Ke, Y.-Y.;Chen, T.-H.;Wang, B.B.-T.;Kuo, S.-J.;Shih, J.-C.;Chen, M.; MING CHEN; JIN-CHUNG SHIH |
| 臺大學術典藏 |
2018-09-10T06:41:40Z |
Comparison of immunohistochemical and fluorescence in situ hybridization assessment for HER-2/neu status in Taiwanese breast cancer patients
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Kuo, S.-J.;Wang, B.B.-T.;Chang, C.-S.;Chen, T.-H.;Yeh, K.-T.;Lee, D.-J.;Yin, P.-L.;Chen, M.; MING CHEN |
| 臺大學術典藏 |
2018-09-10T06:06:47Z |
Prenatal identification of small supernumerary marker chromosomes by FISH in an infant born with mild congenital anomalies [8]
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Chen, M.;Chang, S.-P.;Yin, P.-L.;Sapeta, M.;Barringer, S.;Kuo, S.-J.;Yu, H.-T.;Wang, B.B.-T.; MING CHEN |
| 臺大學術典藏 |
2018-09-10T05:03:07Z |
Prenatal diagnosis of a fetus affected with down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping
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Hsieh, L.-J.;Hsieh, T.-C.;Yeh, G.-P.;Lin, M.-I.;Chen, M.;Wang, B.B.-T.; MING CHEN |
Showing items 1-4 of 4 (1 Page(s) Totally)
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