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

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

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机构	日期	题名	作者
臺大學術典藏	2020-02-20T02:57:00Z	Targeted next-generation sequencing of cancer genes identified frequent TP53 and ATRX mutations in leiomyosarcoma	CHING-YAO YANG; Liau J.-Y.; Huang W.-J.; Chang Y.-T.; Chang M.-C.; Lee J.-C.; Tsai J.-H.; Su Y.-N.; Hung C.-C.; Jeng Y.-M.
臺大學術典藏	2020-02-17T08:07:12Z	PGD of �]-thalassaemia and HLA haplotypes using OmniPlex whole genome amplification	Chen S.-U;Su Y.-N;Fang M.-Y;Chang L.-J;Tsai Y.-Y;Lin L.-T;Lee C.-N;Yu-Shih Yang; Chen S.-U; Su Y.-N; Fang M.-Y; Chang L.-J; Tsai Y.-Y; Lin L.-T; Lee C.-N; YU-SHIH YANG
臺大學術典藏	2020-02-17T08:07:07Z	Preimplantation genetic diagnosis of �]-thalassemia using real-time polymerase chain reaction with fluorescence resonance energy transfer hybridization probes	Hung C.-C; Chen S.-U; Lin S.-Y; Fang M.-Y; Chang L.-J; Tsai Y.-Y; Lin L.-T; YU-SHIH YANG; Lee C.-N; Su Y.-N.
臺大學術典藏	2020-02-17T08:07:06Z	Successful application of the strategy of blastocyst biopsy, vitrification, whole genome amplification, and thawed embryo transfer for preimplantation genetic diagnosis of neurofibromatosis type 1	Chen Y.-L;Hung C.-C;Lin S.-Y;Fang M.-Y;Tsai Y.-Y;Chang L.-J;Lee C.-N;Su Y.-N;Chen S.-U;Yu-Shih Yang; Chen Y.-L; Hung C.-C; Lin S.-Y; Fang M.-Y; Tsai Y.-Y; Chang L.-J; Lee C.-N; Su Y.-N; Chen S.-U; YU-SHIH YANG
臺大學術典藏	2020-02-17T08:07:05Z	An update of preimplantation genetic diagnosis in gene diseases, chromosomal translocation, and aneuploidy screening	Chang L.-J; Chen S.-U; Tsai Y.-Y; Hung C.-C; Fang M.-Y; Su Y.-N; YU-SHIH YANG
臺大學術典藏	2020-02-17T08:07:03Z	Blastocyst biopsy and vitrification are effective for preimplantation genetic diagnosis of monogenic diseases	Chang L.-J; Huang C.-C; Tsai Y.-Y; Hung C.-C; Fang M.-Y; Lin Y.-C; Su Y.-N; Chen S.-U; YU-SHIH YANG
臺大學術典藏	2020-02-17T07:43:43Z	Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM	Lin S.-Y;Su Y.-N;Hung C.-C;Tsay W;Chiou S.-S;Chang C.-T;Hong-Nerng Ho;Lee C.-N.; Lin S.-Y; Su Y.-N; Hung C.-C; Tsay W; Chiou S.-S; Chang C.-T; HONG-NERNG HO; Lee C.-N.
臺大學術典藏	2020-02-17T07:43:41Z	Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis	Hung C.-C;Lin S.-Y;Lee C.-N;Cheng H.-Y;Lin C.-Y;Chang C.-H;Chiu H.-H;Yu C.-C;Lin S.-P;Cheng W.-F;Hong-Nerng Ho;Niu D.-M;Su Y.-N.; Hung C.-C; Lin S.-Y; Lee C.-N; Cheng H.-Y; Lin C.-Y; Chang C.-H; Chiu H.-H; Yu C.-C; Lin S.-P; Cheng W.-F; HONG-NERNG HO; Niu D.-M; Su Y.-N.
臺大學術典藏	2020-02-17T07:43:39Z	Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome	Lin S.-Y; Lee C.-N; Hung C.-C; Tsai W.-Y; Lin S.-P; Li N.-C; Hsieh W.-S; Tung Y.-C; Niu D.-M; Hsu W.-M; Chen L.-Y; Fang M.-Y; Tu M.-P; Kuo P.-W; Lin C.-Y; Su Y.-N; HONG-NERNG HO
臺大學術典藏	2020-02-17T07:43:38Z	Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: A prospective population-based cohort study	Su Y.-N; Hung C.-C; Lin S.-Y; Chen F.-Y; Chern J.P.S; Tsai C; Chang T.-S; Yang C.-C; Li H; HONG-NERNG HO; Lee C.-N.

显示项目 386-395 / 715 (共72页)
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