English  |  正體中文  |  简体中文  |  总笔数 :0  
造访人次 :  51762453    在线人数 :  1138
教育部委托研究计画      计画执行:国立台湾大学图书馆
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
关于TAIR

浏览

消息

著作权

相关连结

"pei lung chen"的相关文件

回到依作者浏览
依题名排序 依日期排序

显示项目 26-50 / 156 (共7页)
<< < 1 2 3 4 5 6 7 > >>
每页显示[10|25|50]项目

机构 日期 题名 作者
臺大學術典藏 2021-07-06T02:04:17Z Replication of an association of a common variant in the Reelin gene (RELN) with schizophrenia in Ashkenazi Jewish women Liu Y.; PEI-LUNG CHEN; McGrath J.; Wolyniec P.; Fallin D.; Nestadt G.; Liang K.-Y.; Pulver A.; Valle D.; Avramopoulos D.
臺大學術典藏 2021-07-06T02:04:17Z Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia PEI-LUNG CHEN; Avramopoulos D.; Lasseter V.K.; McGrath J.A.; Fallin M.D.; Liang K.-Y.; Nestadt G.; Feng N.; Steel G.; Cutting A.S.; Wolyniec P.; Pulver A.E.; Valle D.
臺大學術典藏 2021-07-06T02:04:17Z Familiality of novel factorial dimensions of schizophrenia McGrath J.A.; Avramopoulos D.; Lasseter V.K.; Wolyniec P.S.; Fallin M.D.; Liang K.-Y.; Nestadt G.; Thornquist M.H.; Luke J.R.; PEI-LUNG CHEN; Valle D.; Pulver A.E.
臺大學術典藏 2021-07-06T02:04:16Z Linkage and association on 8p21.2-p21.1 in schizophrenia Fallin M.D.; Lasseter V.K.; Liu Y.; Avramopoulos D.; McGrath J.; Wolyniec P.S.; Nestadt G.; Liang K.-Y.; PEI-LUNG CHEN; Valle D.; Pulver A.E.
臺大學術典藏 2021-07-06T02:04:16Z Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles PEI-LUNG CHEN; Fann C.-S.-J.; Chu C.-C.; Chang C.-C.; Chang S.-W.; Hsieh H.-Y.; Lin M.; Yang W.-S.; Chang T.-C.
臺大學術典藏 2021-07-06T02:04:16Z Clinical implication of the C allele of the ITPKC gene SNP rs28493229 in kawasaki disease: Association with disease susceptibility and BCG scar reactivation Lin M.-T.; Wang J.-K.; Yeh J.-I.; Sun L.-C.; PEI-LUNG CHEN; Wu J.-F.; Chang C.-C.; Lee W.-L.; Shen C.-T.; Wang N.-K.; Wu C.-S.; Yeh S.-Z.; Chen C.-A.; Chiu S.-N.; Wu M.-H.
臺大學術典藏 2021-07-06T02:04:15Z Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment Wu C.-C.; Lin Y.-H.; Lu Y.-C.; Chen P.-J.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏 2021-07-06T02:04:15Z A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease Lin M.-T.; Hsu C.-L.; PEI-LUNG CHEN; Yang W.-S.; Wang J.-K.; Fann C.S.J.; Wu M.-H.
臺大學術典藏 2021-07-06T02:04:15Z Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas Wang C.-P.; Chen T.-C.; Chang Y.-L.; Ko J.-Y.; Yang T.-L.; Lo F.-Y.; Hu Y.-L.; PEI-LUNG CHEN; Wu C.-C.; Lou P.-J.
臺大學術典藏 2021-07-06T02:04:14Z Tuberous sclerosis complex surveillance and management: Recommendations of the 2012 international tuberous sclerosis complex consensus conference Krueger D.A.; Northrup H.; Krueger D.A.; Roberds S.; Smith K.; Sampson J.; Korf B.; Kwiatkowski D.J.; Mowat D.; Nellist M.; Povey S.; de Vries P.; Byars A.; Dunn D.; Ess K.; Hook D.; Jansen A.; King B.; Sahin M.; Whittemore V.; Thiele E.; Bebin E.M.; Chugani H.T.; Crino P.; Curatolo P.; Holmes G.; Nabbout R.; O'Callaghan F.; Wheless J.; Wu J.; Darling T.N.; Cowen E.W.; Gosnell E.; Hebert A.; Mlynarczyk G.; Soltani K.; Teng J.; Wataya-Kaneda M.; Witman P.M.; Kingswood C.; Bissler J.; Budde K.; Hulbert J.; Guay-Woodford L.; Sauter M.; Zonneberg B.; J??wiak S.; Bartels U.; Berhouma M.; Franz D.N.; Koenig M.K.; Roach E.S.; Roth J.; Wang H.; Weiner H.; McCormack F.X.; Almoosa K.; Brody A.; Burger C.; Cottin V.; Finlay G.; Glass J.; Henske E.P.; Johnson S.; Kotloff R.; Lynch D.; Moss J.; Rhu J.; Da Silva A.T.; Young L.R.; Knilans T.; Hinton R.; Prakash A.; Romp R.; Singh A.D.; Debroy A.; PEI-LUNG CHEN; Sparagana S.; Frost M.D.; International Tuberous Sclerosis Complex Consensus Group; PEI-LUNG CHEN
臺大學術典藏 2021-07-06T02:04:14Z Identification of a novel HLA-B allele, B*07:162, in a Taiwanese individual PEI-LUNG CHEN; Lai S.-K.; Yang W.-S.; Chang T.-C.; Chu C.-C.
臺大學術典藏 2021-07-06T02:04:13Z Genetic analysis of CARD14 in non-familial pityriasis rubra pilaris: A case series Hong J.-B.; PEI-LUNG CHEN; Chen Y.-T.; Tsai T.-F.
臺大學術典藏 2021-07-06T02:04:13Z Gene-wide tagging study of the effects of common genetic polymorphisms in the α subunits of the GABAA receptor on epilepsy treatment response Hung C.-C.; PEI-LUNG CHEN; Huang W.-M.; Tai J.J.; Hsieh T.-J.; Ding S.-T.; Hsieh Y.-W.; Liou H.-H.
臺大學術典藏 2021-07-06T02:04:13Z Tuberous sclerosis complex diagnostic criteria update: Recommendations of the 2012 international tuberous sclerosis complex consensus conference Northrup H.; Krueger D.A.; Roberds S.; Smith K.; Sampson J.; Korf B.; Kwiatkowski D.J.; Mowat D.; Nellist M.; Povey S.; de Vries P.; Byars A.; Dunn D.; Ess K.; Hook D.; Jansen A.; King B.; Sahin M.; Whittemore V.; Thiele E.; Bebin E.M.; Chugani H.T.; Crino P.; Curatolo P.; Holmes G.; Nabbout R.; O'Callaghan F.; Wheless J.; Wu J.; Darling T.N.; Cowen E.W.; Gosnell E.; Hebert A.; Mlynarczyk G.; Soltani K.; Teng J.; Wataya-Kaneda M.; Witman P.M.; Kingswood C.; Bissler J.; Budde K.; Hulbert J.; Guay-Woodford L.; Sauter M.; Zonneberg B.; J??wiak S.; Bartels U.; Berhouma M.; Franz D.N.; Koenig M.K.; Roach E.S.; Roth J.; Wang H.; Weiner H.; McCormack F.X.; Almoosa K.; Brody A.; Burger C.; Cottin V.; Finlay G.; Glass J.; Henske E.P.; Johnson S.; Kotloff R.; Lynch D.; Moss J.; Rhu J.; Da Silva A.T.; Young L.R.; Knilans T.; Hinton R.; Prakash A.; Romp R.; Singh A.D.; Debroy A.; PEI-LUNG CHEN; Sparagana S.; Frost M.D.; International Tuberous Sclerosis Complex Consensus Group; PEI-LUNG CHEN
臺大學術典藏 2021-07-06T02:04:12Z Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population Hsieh A.-R.; Chang S.-W.; PEI-LUNG CHEN; Chu C.-C.; Hsiao C.-L.; Yang W.-S.; Chang C.-C.; Wu J.-Y.; Chen Y.-T.; Chang T.-C.; Fann C.S.J.
臺大學術典藏 2021-07-06T02:04:12Z A fault-tolerant method for HLA typing with PacBio data Chang C.-J.; PEI-LUNG CHEN; Yang W.-S.; Chao K.-M.
臺大學術典藏 2021-07-06T02:04:11Z An isodicentric X chromosome with gonadal dysgenesis in a lady without prominent somatic features of Turner's syndrome. A case report Yu T.-Y.; Lin H.-S.; PEI-LUNG CHEN; Huang T.-S.
臺大學術典藏 2021-07-06T02:04:11Z Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing Lin Y.-H.; Wu C.-C.; Hsu T.-Y.; Chiu W.-Y.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏 2021-07-06T02:04:11Z STAT3 mediates regorafenib-induced apoptosis in hepatocellular carcinoma Tai W.-T.; Chu P.-Y.; Shiau C.-W.; Chen Y.-L.; Li Y.-S.; Hung M.-H.; Chen L.-J.; PEI-LUNG CHEN; Su J.-C.; Lin P.-Y.; Yu H.-C.; Chen K.-F.
臺大學術典藏 2021-07-06T02:04:10Z Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling Liu Y.; Pham X.; Zhang L.; PEI-LUNG CHEN; Burzynski G.; McGaughey D.M.; He S.; McGrath J.A.; Wolyniec P.; Fallin M.D.; Pierce M.S.; McCallion A.S.; Pulver A.E.; Avramopoulos D.; Valle D.
臺大學術典藏 2021-07-06T02:04:09Z Identifying children with poor cochlear implantation outcomes using massively parallel sequencing Wu C.-C.; Lin Y.-H.; Liu T.-C.; Lin K.-N.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-M.
臺大學術典藏 2021-07-06T02:04:09Z Association between serum levels of adipocyte fatty acid-binding protein and free thyroxine Tseng F.-Y.; PEI-LUNG CHEN; Chen Y.-T.; Chi Y.-C.; Shih S.-R.; Wang C.-Y.; Chen C.-L.; Yang W.-S.
臺大學術典藏 2021-07-06T02:04:08Z Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study PEI-LUNG CHEN; Shih S.-R.; Wang P.-W.; Lin Y.-C.; Chu C.-C.; Lin J.-H.; Chen S.-C.; Chang C.-C.; Huang T.-S.; Tsai K.S.; Tseng F.-Y.; Wang C.-Y.; Lu J.-Y.; Chiu W.-Y.; Chang C.-C.; Chen Y.-H.; Chen Y.-T.; Fann C.S.-J.; Yang W.-S.; Chang T.-C.
臺大學術典藏 2021-07-06T02:04:08Z Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-K?ster-Hauser syndrome Chen M.-J.; Wei S.-Y.; Yang W.-S.; Wu T.-T.; Li H.-Y.; Ho H.-N.; Yang Y.-S.; PEI-LUNG CHEN
臺大學術典藏 2021-07-06T02:04:07Z Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer Lin P.-H.;Kuo W.-H.;Huang A.-C.;Lu Y.-S.;Lin C.-H.;Kuo S.-H.;Wang M.-Y.;Liu C.-Y.;Cheng F.T.-F.;Yeh M.-H.;Li H.-Y.;Yang Y.-H.;Hsu Y.-H.;Fan S.-C.;Li L.-Y.;Yu S.-L.;Chang K.-J.;Pei-Lung Chen;Ni Y.-H.;Huang C.-S.; Lin P.-H.; Kuo W.-H.; Huang A.-C.; Lu Y.-S.; Lin C.-H.; Kuo S.-H.; Wang M.-Y.; Liu C.-Y.; Cheng F.T.-F.; Yeh M.-H.; Li H.-Y.; Yang Y.-H.; Hsu Y.-H.; Fan S.-C.; Li L.-Y.; Yu S.-L.; Chang K.-J.; PEI-LUNG CHEN; Ni Y.-H.; Huang C.-S.

显示项目 26-50 / 156 (共7页)
<< < 1 2 3 4 5 6 7 > >>
每页显示[10|25|50]项目