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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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Showing items 191-200 of 715  (72 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-12-31T02:57:32Z Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms LING-PING LAI; Su Y.-N.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; Ho Y.-L.; Chen W.-J.; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; Wu M.-H.; Lo H.-M.; Huang S.K.S.; Lin J.-L.
臺大學術典藏 2020-12-31T02:57:31Z Denaturing high-performance liquid chromatography screening for KvLQT1 gene variations in patients with atrial fibrillation LING-PING LAI; Tsai C.-T.; Su Y.-N.; Hwang J.-J.; Lee C.-F.; Hsu K.-L.; Chiang F.-T.; Tseng C.-D.; Tseng Y.-Z.; Lin J.-L.
臺大學術典藏 2020-12-30T08:48:06Z Denaturing high-performance liquid chromatography screening for KvLQT1 gene variations in patients with atrial fibrillation Lai L.-P.; CHIA-TI TSAI; Su Y.-N.; Hwang J.-J.; Lee C.-F.; Hsu K.-L.; Chiang F.-T.; Tseng C.-D.; Tseng Y.-Z.; Lin J.-L.
臺大學術典藏 2020-12-30T08:47:59Z The g.762TC polymorphism of the NPC1L1 gene is common in Chinese and contributes to a higher promoter activity and higher serum cholesterol levels Chen C.-W.; Hwang J.-J.; CHIA-TI TSAI; Su Y.-N.; Hsueh C.-H.; Shen M.J.; Lai L.-P.
臺大學術典藏 2020-12-30T07:47:57Z Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms Ko Y.-L.; Wang C.-C.; Chen W.-J.; Yeh S.-J.; Ho Y.-L.; YEN BIN LIU; Lai L.-P.; Su Y.-N.; Chiang F.-T.; Juang J.-M.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; Wu M.-H.; Lo H.-M.; Huang S.K.S.; Lin J.-L.
臺大學術典藏 2020-12-30T07:47:57Z Erratum: Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms (Journal of Human Genetics (2005) 50 (490-496) DOI: 10.1007/s10038-005-0283-3) Lin J.-L.; Lai L.-P.; Su Y.-N.; Hsieh F.-J.; Chiang F.-T.; Juang J.-M.; YEN BIN LIU; Ho Y.-L.; Chen W.-J.; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; Wu M.-H.; Lo H.-M.; Huang S.K.S.
臺大學術典藏 2020-12-28T12:04:21Z The g.762TC polymorphism of the NPC1L1 gene is common in Chinese and contributes to a higher promoter activity and higher serum cholesterol levels Lai L.-P.; Shen M.J.; Hsueh C.-H.; Su Y.-N.; Tsai C.-T.; HWANG, JUEY-JEN; Chen C.-W.
臺大學術典藏 2020-12-28T10:02:48Z Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis CHIH-CHIEH YU; Chiu H.-H.; Lin C.-Y.; Chang C.-H.; Cheng H.-Y.; Lee C.-N.; Hung C.-C.; Lin S.-Y.; Lin S.-P.; Cheng W.-F.; Ho H.-N.; Niu D.-M.; Su Y.-N.
臺大學術典藏 2020-12-28T10:02:46Z Marfan Syndrome-An Echocardiographer's Perspective Lai L.-P.; Lin J.-L.; Su Y.-N.; CHIH-CHIEH YU
臺大學術典藏 2020-12-28T08:14:42Z Diagnosis of BSEP/ABCB11 Mutations in Asian Patients with Cholestasis Using Denaturing High Performance Liquid Chromatography Chang M.-H.; Wu T.-C.; Hsu H.-Y.; YEN-HSUAN NI; Wu S.-H.; Wang N.-Y.; Su Y.-N.; Liu Y.-J.; Chen H.-L.;Liu Y.-J.;Su Y.-N.;Wang N.-Y.;Wu S.-H.;Yen-Hsuan Ni;Hsu H.-Y.;Wu T.-C.;Chang M.-H.; Chen H.-L.

Showing items 191-200 of 715  (72 Page(s) Totally)
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