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Showing items 486-495 of 715  (72 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-02-12T04:06:02Z Preimplantation genetic diagnosis of �]-thalassemia using real-time polymerase chain reaction with fluorescence resonance energy transfer hybridization probes Su Y.-N.;CHIEN-NAN LEE;Yang Y.-S;Lin L.-T;Tsai Y.-Y;Chang L.-J;Fang M.-Y;Lin S.-Y;Chen S.-U;Hung C.-C; Hung C.-C; Chen S.-U; Lin S.-Y; Fang M.-Y; Chang L.-J; Tsai Y.-Y; Lin L.-T; Yang Y.-S; CHIEN-NAN LEE; Su Y.-N.
臺大學術典藏 2020-02-12T04:06:00Z Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome Ho H.-N.;Su Y.-N;Lin C.-Y;Kuo P.-W;Tu M.-P;Fang M.-Y;Chen L.-Y;Hsu W.-M;Niu D.-M;Tung Y.-C;Hsieh W.-S;Li N.-C;Lin S.-P;Tsai W.-Y;Hung C.-C;CHIEN-NAN LEE;Lin S.-Y; Lin S.-Y; CHIEN-NAN LEE; 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 2020-02-12T04:05:59Z Successful application of the strategy of blastocyst biopsy, vitrification, whole genome amplification, and thawed embryo transfer for preimplantation genetic diagnosis of neurofibromatosis type 1 Yang Y.-S.;Chen S.-U;Su Y.-N;CHIEN-NAN LEE;Chang L.-J;Tsai Y.-Y;Fang M.-Y;Lin S.-Y;Hung C.-C;Chen Y.-L; Chen Y.-L; Hung C.-C; Lin S.-Y; Fang M.-Y; Tsai Y.-Y; Chang L.-J; CHIEN-NAN LEE; Su Y.-N; Chen S.-U; Yang Y.-S.
臺大學術典藏 2020-02-12T04:05:59Z Quantitative and qualitative analyses of the SNRPN gene using real-time PCR with melting curve analysis Su Y.-N.;CHIEN-NAN LEE;Chen L.-Y;Chen C.-P;Lin S.-P;Lin S.-Y;Hung C.-C; Hung C.-C; Lin S.-Y; Lin S.-P; Chen C.-P; Chen L.-Y; CHIEN-NAN LEE; Su Y.-N.
臺大學術典藏 2020-02-12T04:05:58Z Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene Su Y.-N.; Chiou S.-S; Chao M.-C; Su Y.-N.;Chiou S.-S;Chao M.-C;Lin S.-P;Chen C.-P;CHIEN-NAN LEE;Lin S.-Y;Hung C.-C; Hung C.-C; Lin S.-Y; CHIEN-NAN LEE; Chen C.-P; Lin S.-P
臺大學術典藏 2020-02-12T04:05:58Z Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: A prospective population-based cohort study CHIEN-NAN LEE;Ho H.-N;Li H;Yang C.-C;Chang T.-S;Tsai C;Chern J.P.S;Chen F.-Y;Lin S.-Y;Hung C.-C;Su Y.-N; 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; Ho H.-N; CHIEN-NAN LEE
臺大學術典藏 2020-02-12T04:05:57Z Newborn genetic screening for hearing impairment: A preliminary study at a tertiary center Hsu C.-J.;Su Y.-N;CHIEN-NAN LEE;Tsao P.-N;Hsieh W.-S;Lin S.-Y;Hung C.-C;Wu C.-C; Wu C.-C; Hung C.-C; Lin S.-Y; Hsieh W.-S; Tsao P.-N; CHIEN-NAN LEE; Su Y.-N; Hsu C.-J.
臺大學術典藏 2020-02-12T04:05:57Z Two cases of Lowe syndrome presenting as increased fetal nuchal translucency Su Y.-N.;Lin C.-H;Shih J.-C;CHIEN-NAN LEE;Lin S.-Y; Lin S.-Y; CHIEN-NAN LEE; Shih J.-C; Lin C.-H; Su Y.-N.
臺大學術典藏 2020-02-12T04:05:56Z A whole genome methylation analysis of systemic lupus erythematosus: Hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity Ho H.-N.;Su Y.-N;Niu D.-M;Hsieh W.S;Chen L.-Y;Hung C.-C;Chen P.-C;Chuang E.Y;Lai L.-C;Tsai M.-H;CHIEN-NAN LEE;Lin Y.-C;Hsieh S.-C;Lin S.-Y; Lin S.-Y; Hsieh S.-C; Lin Y.-C; CHIEN-NAN LEE; Tsai M.-H; Lai L.-C; Chuang E.Y; Chen P.-C; Hung C.-C; Chen L.-Y; Hsieh W.S; Niu D.-M; Su Y.-N; Ho H.-N.
臺大學術典藏 2020-02-12T04:05:56Z Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH) Su Y.-N.;CHIEN-NAN LEE;Shin J.-C;Lin S.-Y;Lin C.-H;Hung C.-C; Hung C.-C; Lin C.-H; Lin S.-Y; Shin J.-C; CHIEN-NAN LEE; Su Y.-N.

Showing items 486-495 of 715  (72 Page(s) Totally)
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