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機構 日期 題名 作者
臺大學術典藏 2020-12-24T06:16:57Z Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints Ke Y.-Y.; Wang T.-J.; Lee D.-J.; Ma G.-C.; Lee N.-C.; Chen M.; YIN-HSIU CHIEN; Hwu W.-L.
臺大學術典藏 2020-12-16T02:25:44Z Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints Lee N.-C.;Chen M.;Ma G.-C.;Lee D.-J.;Wang T.-J.;Ke Y.-Y.;Chien Y.-H.;Wuh-Liang Hwu; Lee N.-C.; Chen M.; Ma G.-C.; Lee D.-J.; Wang T.-J.; Ke Y.-Y.; Chien Y.-H.; WUH-LIANG HWU
臺大學術典藏 2020-12-16T02:25:39Z Experimental treatment of bilateral fetal chylothorax using in-utero pleurodesis Yang Y.-S.; Ma G.-C.; Shih J.-C.; Chen C.-P.; Chou C.-H.; Yeh K.-T.; Kuo S.-J.; Chen T.-H.; WUH-LIANG HWU; Lee T.-H.; Chen M.
臺大學術典藏 2020-12-16T02:25:39Z Preimplantation and prenatal genetic diagnosis of aromatic L-amino aciddecarboxylase deficiency with an amplification refractory mutation system-quantitative polymerase chain reaction Kuo S.-J.;Ma G.-C.;Chang S.-P.;Wu H.-H.;Chen C.-P.;Chang T.-M.;Lin W.-H.;Wu S.-H.;Lee M.-H.;Wuh-Liang Hwu;Chen M.; Kuo S.-J.; Ma G.-C.; Chang S.-P.; Wu H.-H.; Chen C.-P.; Chang T.-M.; Lin W.-H.; Wu S.-H.; Lee M.-H.; WUH-LIANG HWU; Chen M.
臺大學術典藏 2020-12-16T02:25:37Z Genome-wide gene expression analysis implicates the immune response and lymphangiogenesis in the pathogenesis of fetal chylothorax Yeang C.-H.; Ma G.-C.; Shih J.-C.; Yang Y.-S.; Chen C.-P.; Chang S.-P.; Wu S.-H.; Liu C.-S.; Kuo S.-J.; Chou H.-C.; WUH-LIANG HWU; Cameron A.D.; Ginsberg N.A.; Lin Y.-S.; Chen M.
臺大學術典藏 2020-12-09T01:38:34Z Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints Ni-Chung Lee;Chen M.;Ma G.-C.;Lee D.-J.;Wang T.-J.;Ke Y.-Y.;Chien Y.-H.;Hwu W.-L.; NI-CHUNG LEE; Chen M.; Ma G.-C.; Lee D.-J.; Wang T.-J.; Ke Y.-Y.; Chien Y.-H.; Hwu W.-L.
臺大學術典藏 2020-11-27T08:14:26Z Proinflammatory macrophage migratory inhibition factor and interleukin-6 are concentrated in pleural effusion of human fetuses with prenatal chylothorax Chen M.;Chang-Yao Hsieh;Shih J.-C.;Chou C.-H.;Ma G.-C.;Chen T.-H.;Lee T.-H.;Tsai H.-D.;Cameron A.D.;Chen C.-P.; Chen M.; CHANG-YAO HSIEH; Shih J.-C.; Chou C.-H.; Ma G.-C.; Chen T.-H.; Lee T.-H.; Tsai H.-D.; Cameron A.D.; Chen C.-P.
臺大學術典藏 2020-03-03T02:33:33Z Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonography Ma G.-C.; Chang S.-D.; Chang Y.; Chang S.-P.; Yang C.-W.; MING-JEN LEE; Lee T.-H.; Chen M.
臺大學術典藏 2020-03-02T08:11:04Z Preimplantation genetic diagnosis and screening: Current status and future challenges Chen H.-F.; Chen S.-U.; Ma G.-C.; SUNG-TSANG HSIEH; Tsai H.-D.; Yang Y.-S.; Chen M.
臺大學術典藏 2020-03-02T08:11:01Z Preimplantation genetic diagnosis of neurodegenerative diseases: Review of methodologies and report of our experience as a regional reference laboratory Liao C.-H.;Chang M.-Y.;Ma G.-C.;Chang S.-P.;Lin C.-F.;Lin W.-H.;Chen H.-F.;Chen S.-U.;Lee Y.-C.;Chao C.-C.;Chen M.;Sung-Tsang Hsieh; Liao C.-H.; Chang M.-Y.; Ma G.-C.; Chang S.-P.; Lin C.-F.; Lin W.-H.; Chen H.-F.; Chen S.-U.; Lee Y.-C.; Chao C.-C.; Chen M.; SUNG-TSANG HSIEH

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