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Nature Genetics|January 12, 2010
Genome-wide association study of PR intervalArne Pfeufer, Charlotte van Noord, Kristin D Marciante, et al.Nature Genetics|January 12, 2010
Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci, John D Reveille, Anne-Marie Sims, et al.Nature Genetics|December 17, 2009
Genome-wide association study identifies five loci associated with lung functionEmmanouela Repapi, Ian Sayers, Louise V Wain, et al.Nature Genetics|January 1, 1994
Direct isolation of polymorphic markers linked to a trait by genetically directed representational difference analysisN A Lisitsyn, J A Segre, K Kusumi, et al.Nature Genetics|June 1, 1993
Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosisA Blumenfeld, S A Slaugenhaupt, F B Axelrod, et al.Nature Genetics|June 1, 1993
Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplificationH Caron, P van Sluis, M van Hoeve, et al.Nature Genetics|February 1, 1994
A second Ewing's sarcoma translocation, t(21;22), fuses the EWS gene to another ETS-family transcription factor, ERGP H Sorensen, S L Lessnick, D Lopez-Terrada, et al.Nature Genetics|November 1, 2005
An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data setsEleftheria Zeggini, William Rayner, Andrew P Morris, et al.Nature Genetics|October 18, 2005
Mutations in dynamin 2 cause dominant centronuclear myopathyMarc Bitoun, Svetlana Maugenre, Pierre-Yves Jeannet, et al.Nature Genetics|May 2, 2002
Polygenic susceptibility to breast cancer and implications for preventionPaul D P Pharoah, Antonis Antoniou, Martin Bobrow, et al.Pageof 744