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機構 日期 題名 作者
臺大學術典藏 2020-02-12T04:06:26Z Denaturing HPLC coupled with multiplex PCR for rapid detection of large deletions in Duchenne muscular dystrophy carriers Yang C.-C; Lee W.-T; Chien S.-C; Lin W.-L; CHIEN-NAN LEE; CHIEN-NAN LEE;Lin W.-L;Chien S.-C;Lee W.-T;Yang C.-C;Lin C.-Y;Su Y.-N;Hung C.-C; Hung C.-C; Su Y.-N; Lin C.-Y
臺大學術典藏 2020-02-12T04:06:19Z A rapid and reliable detection system for the analysis of PMP22 gene dosage by MP/DHPLC assay Hsieh S.-T.;Chen C.-A;Lin W.-L;Cheng W.-F;Hung C.-C;CHIEN-NAN LEE;Su Y.-N;Lin C.-Y; Lin C.-Y; Su Y.-N; CHIEN-NAN LEE; Hung C.-C; Cheng W.-F; Lin W.-L; Chen C.-A; Hsieh S.-T.
臺大學術典藏 2020-02-12T04:06:16Z Molecular and clinical analyses of 84 patients with tuberous sclerosis complex CHIEN-NAN LEE;Lin W.-L;Lee W.-T;Chen C.-P;Hsieh C.-J;Chen P.-C;Chen C.-C;Liou H.-H;Chien S.-C;Su Y.N;Hung C.-C; Hung C.-C; Su Y.N; Chien S.-C; Liou H.-H; Chen C.-C; Chen P.-C; Hsieh C.-J; Chen C.-P; Lee W.-T; Lin W.-L; CHIEN-NAN LEE
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 2020-02-12T04:06:08Z Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison Lin W.-L.;Su Y.-N;Jong Y.-J;Yang C.-C;Hsieh S.-T;Chen C.-A;Cheng W.-F;Lin C.-Y;CHIEN-NAN LEE;Hung C.-C; Hung C.-C; CHIEN-NAN LEE; Lin C.-Y; Cheng W.-F; Chen C.-A; Hsieh S.-T; Yang C.-C; Jong Y.-J; Su Y.-N; Lin W.-L.
臺大學術典藏 2020-02-12T04:06:06Z Comparison of the mismatch-specific endonuclease method and denaturing high-performance liquid chromatography for the identification of HBB gene mutations Hung C.-C; Su Y.-N; Lin C.-Y; Chang Y.-F; Chang C.-H; Cheng W.-F; Chen C.-A; CHIEN-NAN LEE; Lin W.-L.; Lin W.-L.;CHIEN-NAN LEE;Chen C.-A;Cheng W.-F;Chang C.-H;Chang Y.-F;Lin C.-Y;Su Y.-N;Hung C.-C
臺大學術典藏 2020-02-12T04:06:04Z Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR Lin S.-P; Niu D.-M; Lee N.-C; Cheng W.-F; Chen C.-P; Lin W.-L; CHIEN-NAN LEE; Su Y.-N.; Su Y.-N.;CHIEN-NAN LEE;Lin W.-L;Chen C.-P;Cheng W.-F;Lee N.-C;Niu D.-M;Lin S.-P;Lin S.-Y;Hung C.-C; Hung C.-C; Lin S.-Y

顯示項目 121-130 / 281 (共29頁)
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