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

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	造訪人次 : 53584655 線上人數 : 841 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	2020-02-14T02:50:08Z	Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: Application in prader-willi syndrome and duchenne muscular dystrophy	Lin W.-L.; Su Y.-N.; Liu M.S.; Hsieh W.-S.; WEN-FANG CHENG; Lee C.-N.; Chien S.-C.; Lin S.-P.; Chen C.-P.; Hung C.-C.; Hung C.-C.;Chen C.-P.;Lin S.-P.;Chien S.-C.;Lee C.-N.;Wen-Fang Cheng;Hsieh W.-S.;Liu M.S.;Su Y.-N.;Lin W.-L.
臺大學術典藏	2020-02-12T04:06:34Z	Placenta Growth Factor Elevation in the Cord Blood of Premature Neonates Predicts Poor Pulmonary Outcome	Hsieh F.-J.;Hsieh W.-S;Chou H.-C;CHIEN-NAN LEE;Su Y.-N;Wei S.-C;Tsao P.-N; Tsao P.-N; Wei S.-C; Su Y.-N; CHIEN-NAN LEE; Chou H.-C; Hsieh W.-S; Hsieh F.-J.
臺大學術典藏	2020-02-12T04:06:31Z	Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: A highly efficient and reliable carrier-screening test	Hsu S.-M.;Lin W.-L;Hsieh W.-S;Yu C.-L;Chang M.-C;Tsao P.-N;Cheng W.-F;CHIEN-NAN LEE;Li H;Hung C.-C;Su Y.-N; Su Y.-N; Hung C.-C; Li H; CHIEN-NAN LEE; Cheng W.-F; Tsao P.-N; Chang M.-C; Yu C.-L; Hsieh W.-S; Lin W.-L; Hsu S.-M.
臺大學術典藏	2020-02-12T04:06:13Z	Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: Application in prader-willi syndrome and duchenne muscular dystrophy	Lin W.-L.;Su Y.-N;Liu M.S;Hsieh W.-S;Cheng W.-F;CHIEN-NAN LEE;Chien S.-C;Lin S.-P;Chen C.-P;Hung C.-C; Hung C.-C; Chen C.-P; Lin S.-P; Chien S.-C; CHIEN-NAN LEE; Cheng W.-F; Hsieh W.-S; Liu M.S; Su Y.-N; Lin W.-L.
臺大學術典藏	2020-02-12T04:06:11Z	Molecular assay of -�\3.7 and -�\4.2 deletions causing �\-thalassemia by denaturing high-performance liquid chromatography	Hsu S.-M.;Su Y.-N;Lin W.-L;Hsieh W.-S;Jong Y.-J;Chen C.-P;CHIEN-NAN LEE;Hung C.-C; Hung C.-C; CHIEN-NAN LEE; Chen C.-P; Jong Y.-J; Hsieh W.-S; Lin W.-L; Su Y.-N; Hsu S.-M.
臺大學術典藏	2020-02-12T04:06:10Z	Use of multiplex PCR and CE for gene dosage quantification and its biomedical application for SMN, PMP22, and �\-globin genes	Su Y.-N.;CHIEN-NAN LEE;Lin W.-L;Liu M.S;Hsieh W.-S;Hsieh S.-T;Jong Y.-J;Chang Y.-F;Chang C.-H;Lin C.-Y;Chien S.-C;Hung C.-C; Hung C.-C; Chien S.-C; Lin C.-Y; Chang C.-H; Chang Y.-F; Jong Y.-J; Hsieh S.-T; Hsieh W.-S; Liu M.S; Lin W.-L; CHIEN-NAN LEE; Su Y.-N.
臺大學術典藏	2020-02-12T04:06:08Z	Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis	Lin W.-L.;Su Y.-N;Hsieh W.-S;Chen C.-P;Jong Y.-J;Chang C.-H;CHIEN-NAN LEE;Hung C.-C; Hung C.-C; CHIEN-NAN LEE; Chang C.-H; Jong Y.-J; Chen C.-P; Hsieh W.-S; Su Y.-N; Lin W.-L.
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	2020-02-12T04:05:57Z	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	2020-02-12T04:05:56Z	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.

顯示項目 566-575 / 779 (共78頁)
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