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Showing items 176-200 of 715 (29 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2021-01-06T03:38:55Z	Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum	Lee C.-T.; Tung Y.-C.; Hwu W.-L.; Shih J.-C.; Lin W.-H.; Wu M.-Z.; Kuo K.-T.; YUNG-LI YANG; Chen H.-L.; Chen M.; Su Y.-N.; Jong Y.-J.; Liu S.-Y.; Tsai W.-Y.; Lee N.-C.
臺大學術典藏	2021-01-06T03:38:54Z	TP53 alterations in relapsed childhood acute lymphoblastic leukemia	Lin K.-H.; Lin C.-Y.; Lin T.-K.; Chang Y.-H.; Jou S.-T.; Chang W.-T.; Yu C.-H.; Lu M.-Y.; Chen S.-H.; Wu K.-H.; Wang S.-C.; Chang H.-H.; Su Y.-N.; Hung C.-C.; Lin D.-T.; Chen H.-Y.; YUNG-LI YANG
臺大學術典藏	2021-01-06T03:38:51Z	MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia	Lu M.-Y.; Chen S.-H.; Cheng C.-N.; Wu K.-H.; Wang S.-C.; Chang H.-H.; Li M.-J.; Ni Y.-L.; Su Y.-N.; Lin D.-T.; Chen H.-Y.; Harrison C.J.; Hung C.-C.; Lin S.-W.; YUNG-LI YANG; Yu C.-H.; Lin T.-K.; Jou S.-T.; Lin C.-Y.; Lin K.-H.
臺大學術典藏	2021-01-05T08:07:44Z	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	Lo H.-M.; Huang S.K.S.; Lin J.-L.; Lai L.-P.;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.;Mei-Hwan Wu;Lo H.-M.;Huang S.K.S.;Lin J.-L.; Lai L.-P.; 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.; MEI-HWAN WU
臺大學術典藏	2021-01-05T08:07:39Z	Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases	Lee C.-N.;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Wang J.-K.;Mei-Hwan Wu;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; Cheng W.-F.; Lin M.-T.; Wang J.-K.; MEI-HWAN WU; Hsieh F.-J.
臺大學術典藏	2021-01-05T08:07:36Z	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)	Huang S.K.S.; Lo H.-M.; MEI-HWAN WU; Lin T.-K.; Chen S.-A.; Tsao H.-M.; Lei M.-H.; Lai L.-P.; Su Y.-N.; Hsieh F.-J.; 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.; Lin J.-L.
臺大學術典藏	2021-01-05T06:41:16Z	Novel neurotrophic tyrosine kinase receptor type 1 gene mutation associated with congenital insensitivity to pain with anhidrosis	Lin Y.-P.;Su Y.-N.;Wen-Chin Weng;Lee W.-T.; Lin Y.-P.; Su Y.-N.; WEN-CHIN WENG; Lee W.-T.
臺大學術典藏	2021-01-05T06:41:09Z	The relationship of neuroimaging findings and neuropsychiatric comorbidities in children with tuberous sclerosis complex	Huang C.-H.; Huang C.-H.;Peng S.S.F.;Wen-Chin Weng;Su Y.-N.;Lee W.-T.;National Taiwan University Hospital Tuberous Sclerosis Complex (Ntuh Tsc) Study Group; Peng S.S.F.; WEN-CHIN WENG; Su Y.-N.; Lee W.-T.; National Taiwan University Hospital Tuberous Sclerosis Complex (NTUH TSC) Study Group
臺大學術典藏	2021-01-05T02:29:04Z	Impact of a National β-Thalassemia Carrier Screening Program on the birth rate of thalassemia major	Lin D.-T.; SHIANN-TANG JOU; Lu M.-Y.; Su Y.-N.; Lin K.-H.; Chern J.P.S.; Lin K.-S.; Wang S.-C.
臺大學術典藏	2021-01-05T02:28:44Z	TP53 alterations in relapsed childhood acute lymphoblastic leukemia	Lin C.-Y.; Chang Y.-H.; Lin T.-K.; SHIANN-TANG JOU; Chang W.-T.; Yu C.-H.; Yang Y.-L.; Chen H.-Y.; Lin K.-H.; Lu M.-Y.; Chen S.-H.; Wu K.-H.; Wang S.-C.; Chang H.-H.; Su Y.-N.; Hung C.-C.; Lin D.-T.
臺大學術典藏	2021-01-04T07:36:08Z	Prenatal diagnosis of progressive familial intrahepatic cholestasis type 2	Chen S.-T.;Chen H.-L.;Su Y.-N.;Liu Y.-J.;Ni Y.-H.;Hsu H.-Y.;Chu C.-S.;Wang N.-Y.;Mei-Hwei Chang; Chen S.-T.; Chen H.-L.; Su Y.-N.; Liu Y.-J.; Ni Y.-H.; Hsu H.-Y.; Chu C.-S.; Wang N.-Y.; MEI-HWEI CHANG
臺大學術典藏	2021-01-04T07:33:51Z	211 G to A variation of UDP-glucuronosyl transferase 1A1 gene and neonatal Breastfeeding jaundice	Tsao P.-N.; MEI-HWEI CHANG; Chou H.-C.;Chen M.-H.;Yang H.-I.;Su Y.-N.;Hsieh W.-S.;Chen C.-Y.;Chen H.-L.;Mei-Hwei Chang;Tsao P.-N.; Chou H.-C.; Chen M.-H.; Yang H.-I.; Su Y.-N.; Hsieh W.-S.; Chen C.-Y.; Chen H.-L.
臺大學術典藏	2021-01-04T07:33:46Z	Diagnosis of neonatal intrahepatic cholestasis caused by citrin deficiency using high-resolution melting analysis and a clinical scoring system	Chen S.-T.; Su Y.-N.; Ni Y.-H.; Hwu W.-L.; Lee N.-C.; Chien Y.-H.; Chang C.-C.; Chen H.-L.; MEI-HWEI CHANG
臺大學術典藏	2021-01-04T07:32:13Z	Decreased neonatal hepatitis B virus (HBV) viremia by maternal tenofovir treatment predicts reduced chronic HBV infection in children born to highly viremic mothers	Chen H.-J.; Lin Y.-H.; Chang Y.-K.; Chen K.-H.; Yang C.-K.; Zhao L.-L.; Chang K.-C.; MEI-HWEI CHANG; Lee C.-N.; Chang C.-H.; Wu J.-F.; Ni Y.-H.; Wen W.-H.; Shyu M.-K.; Lai M.-W.; Chen S.-M.; Hu J.-J.; Lin H.H.; Hsu J.-J.; Mu S.-C.; Lin Y.-C.; Liu C.-J.; Chen D.-S.; Lin L.-H.; Chen H.-L.; Hwa H.-L.; Su Y.-N.; Shih J.-C.; Chao K.-H.; Hsu H.-Y.; Chiu Y.-C.; Su T.-H.; Lin C.-C.; Lin P.-Y.; Yang W.-R.; The Taiwan Study Group for the Prevention of Mother-to-Infant Transmission of HBV (PreMIT study); Pan H.-S.; Lau B.-H.; Lee C.-L.; Cheng P.-J.; Chang Y.-L.; Chiueh H.-Y.; Wang T.-H.; Lo L.-M.; Hsieh C.-L.; Cheng S.-W.; Tsai M.-S.; She B.-Q.; Koh K.-J.; Hung Y.-L.; Lin H.-M.; Peng F.-S.; Wu T.-C.; Chen C.-Y.; Chen C.-P.; Huang J.-P.; Yeung C.-Y.; Lin C.-J.; Chiu W.-T.; Wang D.-S.; Lin W.-T.; Hwang K.-S.; Huang C.-F.
臺大學術典藏	2021-01-04T07:32:09Z	Long-term growth and bone development in children of HBV-infected mothers with and without fetal exposure to tenofovir disoproxil fumarate	Shih J.C.; Su Y.N.; Shyu M.K.; Hwa H.L.; MEI-HWEI CHANG; Wen W.-H.; Chen H.-L.; Shih T.T.-F.; Wu J.-F.; Ni Y.-H.; Lee C.-N.; Zhao L.-L.; Lai M.-W.; Mu S.-C.; Tung Y.-C.; Hsu H.-Y.; Chao K.H.; Chiu Y.C.; Chang K.C.; Liu C.J.; Su T.H.; Chen D.S.; Chen S.M.; Lin C.C.; Lin P.Y.; Yang W.R.; Hu J.J.; Yang C.K.; Chang Y.K.; Chen K.H.; Lin H.H.; Lin Y.H.; Chen H.J.; Pan H.S.; Lau B.H.; Lee C.L.; Cheng P.J.; Chang Y.L.; Chiueh H.Y.; Wang T.H.; Hsu J.J.; Lo L.M.; Hsieh C.L.; Cheng S.W.; Tsai M.S.; Lin L.H.; She B.Q.; Peng F.S.; Lin Y.C.; Chen C.P.; Huang J.P.; Yeung C.Y.; Taiwan Study Group for the Prevention of Mother-to-Infant Transmission of HBV (PreMIT study)
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 176-200 of 715 (29 Page(s) Totally)
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