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	2020-02-10T06:49:26Z	Preimplantation genetic diagnosis (embryo screening) for enlarged vestibular aqueduct due to SLC26A4 mutation	Wu C.-C;Shin-Yu Lin;Su Y.-N;Fang M.-Y;Chen S.-U;Hsu C.-J.; Wu C.-C; SHIN-YU LIN; Su Y.-N; Fang M.-Y; Chen S.-U; Hsu C.-J.
臺大學術典藏	2020-02-10T06:49:24Z	Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations	Chen C.-P;Su Y.-N;Shin-Yu Lin;Chang C.-L;Wang Y.-L;Huang J.-P;Chen C.-Y;Hung F.-Y;Chen Y.-Y;Wu P.-C;Wang W.; Chen C.-P; Su Y.-N; SHIN-YU LIN; Chang C.-L; Wang Y.-L; Huang J.-P; Chen C.-Y; Hung F.-Y; Chen Y.-Y; Wu P.-C; Wang W.
臺大學術典藏	2020-02-10T06:49:24Z	Quantitative and qualitative analyses of the SNRPN gene using real-time PCR with melting curve analysis	Hung C.-C;Shin-Yu Lin;Lin S.-P;Chen C.-P;Chen L.-Y;Lee C.-N;Su Y.-N.; Hung C.-C; SHIN-YU LIN; Lin S.-P; Chen C.-P; Chen L.-Y; Lee C.-N; Su Y.-N.
臺大學術典藏	2020-02-10T06:49:24Z	Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome	Shin-Yu Lin;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;Ho H.-N.; SHIN-YU LIN; 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; Ho H.-N.
臺大學術典藏	2020-02-10T06:49:23Z	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;Shin-Yu Lin;Chen F.-Y;Chern J.P.S;Tsai C;Chang T.-S;Yang C.-C;Li H;Ho H.-N;Lee C.-N.; Su Y.-N; Hung C.-C; SHIN-YU LIN; Chen F.-Y; Chern J.P.S; Tsai C; Chang T.-S; Yang C.-C; Li H; Ho H.-N; Lee C.-N.
臺大學術典藏	2020-02-10T06:49:23Z	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;Shin-Yu Lin;Fang M.-Y;Tsai Y.-Y;Chang L.-J;Lee C.-N;Su Y.-N;Chen S.-U;Yang Y.-S.; Chen Y.-L; Hung C.-C; SHIN-YU LIN; Fang M.-Y; Tsai Y.-Y; Chang L.-J; Lee C.-N; Su Y.-N; Chen S.-U; Yang Y.-S.
臺大學術典藏	2020-02-10T06:49:22Z	Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene	Hung C.-C;Shin-Yu Lin;Lee C.-N;Chen C.-P;Lin S.-P;Chao M.-C;Chiou S.-S;Su Y.-N.; Hung C.-C; SHIN-YU LIN; Lee C.-N; Chen C.-P; Lin S.-P; Chao M.-C; Chiou S.-S; Su Y.-N.
臺大學術典藏	2020-02-10T06:49:21Z	Prenatal diagnosis of mosaic trisomy 2: Discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction	Chen C.-P;Su Y.-N;Shin-Yu Lin;Chern S.-R;Chen Y.-T;Lee M.-S;Wang W.; Chen C.-P; Su Y.-N; SHIN-YU LIN; Chern S.-R; Chen Y.-T; Lee M.-S; Wang W.
臺大學術典藏	2020-02-10T06:49:21Z	Newborn genetic screening for hearing impairment: A preliminary study at a tertiary center	Wu C.-C;Hung C.-C;Shin-Yu Lin;Hsieh W.-S;Tsao P.-N;Lee C.-N;Su Y.-N;Hsu C.-J.; Wu C.-C; Hung C.-C; SHIN-YU LIN; Hsieh W.-S; Tsao P.-N; Lee C.-N; Su Y.-N; Hsu C.-J.
臺大學術典藏	2020-02-10T06:49:21Z	Two cases of Lowe syndrome presenting as increased fetal nuchal translucency	Shin-Yu Lin;Lee C.-N;Shih J.-C;Lin C.-H;Su Y.-N.; SHIN-YU LIN; Lee C.-N; Shih J.-C; Lin C.-H; Su Y.-N.

显示项目 516-525 / 715 (共72页)
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