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Institution Date Title Author
臺大學術典藏 2020-12-16T02:26:03Z Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype Chen M.;Wuh-Liang Hwu;Kuo S.-J.;Chen C.-P.;Yin P.-L.;Chang S.-P.;Lee D.-J.;Chen T.-H.;Wang B.-T.;Lin C.-C.; Chen M.; WUH-LIANG HWU; Kuo S.-J.; Chen C.-P.; Yin P.-L.; Chang S.-P.; Lee D.-J.; Chen T.-H.; Wang B.-T.; Lin C.-C.
臺大學術典藏 2018-09-10T06:41:41Z Diagnostic confirmation of X-linked recessive ichthyosis by fluorescent in situ hybridization - A case report Ho, C.-Y.;Yang, K.-C.;Chen, M.;Chang, S.-P.;Yin, P.-L.; MING CHEN
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 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] Chen, M.;Chang, S.-P.;Yin, P.-L.;Sapeta, M.;Barringer, S.;Kuo, S.-J.;Yu, H.-T.;Wang, B.B.-T.; MING CHEN

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