臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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	造訪人次 : 51992552 線上人數 : 789 教育部委託研究計畫計畫執行:國立臺灣大學圖書館

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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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機構	日期	題名	作者
臺大學術典藏	2020-02-17T08:07:00Z	Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: Validation and verification	YU-SHIH YANG; Chang S.-P; Chen H.-F; Ma G.-C; Lin W.-H; Lin C.-F; Tsai F.-P; Wu C.-H; Tsai H.-D; Lee T.-H; Chen M.
臺大學術典藏	2020-02-17T08:06:59Z	A pilot proof-of-principle study to compare fresh and vitrified cycle preimplantation genetic screening by chromosome microarray and next generation sequencing	Chen M.; Chiu C; Lin C.-F; Tsai F.-P; Lin W.-H; Ma G.-C; Chen H.-F; YU-SHIH YANG
臺大學術典藏	2020-02-17T08:06:59Z	A pilot proof-of-principle study to compare fresh and vitrified cycle preimplantation genetic screening by chromosome microarray and next generation sequencing	Ma G.-C; Chen H.-F; YU-SHIH YANG; Lin W.-H; Tsai F.-P; Lin C.-F; Chiu C; Chen M.
臺大學術典藏	2020-02-17T08:06:57Z	Preimplantation genetic diagnosis and screening: Current status and future challenges	Chen S.-U; Chen H.-F; Chen H.-F;Chen S.-U;Ma G.-C;Hsieh S.-T;Tsai H.-D;Yu-Shih Yang;Chen M.; Ma G.-C; Hsieh S.-T; Tsai H.-D; YU-SHIH YANG; Chen M.
臺大學術典藏	2020-02-17T08:06:57Z	Preimplantation genetic diagnosis and screening: Current status and future challenges	Chen H.-F;Chen S.-U;Ma G.-C;Hsieh S.-T;Tsai H.-D;Yu-Shih Yang;Chen M.; Chen H.-F; Chen S.-U; Ma G.-C; Hsieh S.-T; Tsai H.-D; YU-SHIH YANG; Chen M.
臺大學術典藏	2020-02-12T04:05:37Z	Application of molecular cytogenetic techniques to characterize the aberrant Y chromosome arising de novo in a male fetus with mosaic 45,X and solve the discrepancy between karyotyping, chromosome microarray, and multiplex ligation dependent probe amplification	Chen M.;Ma G.-C;Lin W.-H;Lee D.-J;Yuan T.-J;Peng A.-Y;CHIEN-NAN LEE;Lin S.-Y; Lin S.-Y; CHIEN-NAN LEE; Peng A.-Y; Yuan T.-J; Lee D.-J; Lin W.-H; Ma G.-C; Chen M.
臺大學術典藏	2020-02-10T06:49:07Z	Application of molecular cytogenetic techniques to characterize the aberrant Y chromosome arising de novo in a male fetus with mosaic 45,X and solve the discrepancy between karyotyping, chromosome microarray, and multiplex ligation dependent probe amplification	Shin-Yu Lin;Lee C.-N;Peng A.-Y;Yuan T.-J;Lee D.-J;Lin W.-H;Ma G.-C;Chen M.; SHIN-YU LIN; Lee C.-N; Peng A.-Y; Yuan T.-J; Lee D.-J; Lin W.-H; Ma G.-C; Chen M.
臺大學術典藏	2020-02-06T06:49:52Z	Preimplantation genetic diagnosis and screening: Current status and future challenges	Chen H.-F;Shee-Uan Chen;Ma G.-C;Hsieh S.-T;Tsai H.-D;Yang Y.-S;Chen M.; Chen H.-F; SHEE-UAN CHEN; Ma G.-C; Hsieh S.-T; Tsai H.-D; Yang Y.-S; Chen M.
臺大學術典藏	2020-02-06T06:49:51Z	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;Shee-Uan Chen;Lee Y.-C;Chao C.-C;Chen M;Hsieh S.-T.; Liao C.-H; Chang M.-Y; Ma G.-C; Chang S.-P; Lin C.-F; Lin W.-H; Chen H.-F; SHEE-UAN CHEN; Lee Y.-C; Chao C.-C; Chen M; Hsieh S.-T.
臺大學術典藏	2020-01-22T07:50:33Z	Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization	Chen M.;Yang Y.-S.;Shih J.-C.;Lin W.-H.;Lee D.-J.;Lin Y.-S.;Chou C.-H.;Cameron A.D.;Ginsberg N.A.;Chi-An Chen;Lee M.-L.;Ma G.-C.; Chen M.; Yang Y.-S.; Shih J.-C.; Lin W.-H.; Lee D.-J.; Lin Y.-S.; Chou C.-H.; Cameron A.D.; Ginsberg N.A.; CHI-AN CHEN; Lee M.-L.; Ma G.-C.

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