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Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes.
Ingles, Jodie; Goldstein, Jennifer; Thaxton, Courtney; Caleshu, Colleen; Corty, Edward W; Crowley, Stephanie B; Dougherty, Kristen; Harrison, Steven M; McGlaughon, Jennifer; Milko, Laura V; Morales, Ana; Seifert, Bryce A; Strande, Natasha; Thomson, Kate; Peter van Tintelen, J; Wallace, Kathleen; Walsh, Roddy; Wells, Quinn; Whiffin, Nicola; Witkowski, Leora; Semsarian, Christopher; Ware, James S; Hershberger, Ray E; Funke, Birgit.
Affiliation
  • Ingles J; Agnes Ginges Centre for Molecular Cardiology at Centenary Institute and Faculty of Medicine and Health, The University of Sydney, University of Sydney, Australia (J.I., C.S.).
  • Goldstein J; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, Australia (J.I., C.S.).
  • Thaxton C; Department of Genetics, UNC Chapel Hill, NC (J.G., C.T., E.W.C., S.B.C., J.M., L.V.M., B.A.S., N.S., K.W.).
  • Caleshu C; Department of Genetics, UNC Chapel Hill, NC (J.G., C.T., E.W.C., S.B.C., J.M., L.V.M., B.A.S., N.S., K.W.).
  • Corty EW; Stanford Center for Inherited Cardiovascular Disease, Stanford University, CA (C.C.).
  • Crowley SB; Department of Genetics, UNC Chapel Hill, NC (J.G., C.T., E.W.C., S.B.C., J.M., L.V.M., B.A.S., N.S., K.W.).
  • Dougherty K; Department of Genetics, UNC Chapel Hill, NC (J.G., C.T., E.W.C., S.B.C., J.M., L.V.M., B.A.S., N.S., K.W.).
  • Harrison SM; Eastern Virginia Medical School, Norfolk, VA (K.D.).
  • McGlaughon J; Laboratory for Molecular Medicine, Partners Healthcare, Harvard Medical School, Cambridge, MA (S.M.H.).
  • Milko LV; Department of Genetics, UNC Chapel Hill, NC (J.G., C.T., E.W.C., S.B.C., J.M., L.V.M., B.A.S., N.S., K.W.).
  • Morales A; Department of Genetics, UNC Chapel Hill, NC (J.G., C.T., E.W.C., S.B.C., J.M., L.V.M., B.A.S., N.S., K.W.).
  • Seifert BA; Division of Human Genetics, Davis Heart and Lung Research Institute (A.M., R.E.H.).
  • Strande N; Department of Genetics, UNC Chapel Hill, NC (J.G., C.T., E.W.C., S.B.C., J.M., L.V.M., B.A.S., N.S., K.W.).
  • Thomson K; Department of Genetics, UNC Chapel Hill, NC (J.G., C.T., E.W.C., S.B.C., J.M., L.V.M., B.A.S., N.S., K.W.).
  • Peter van Tintelen J; Oxford Medical Genetics Laboratory, United Kingdom (K.T.).
  • Wallace K; Department of Clinical Genetics, Amsterdam University Medical Centers, University of Amsterdam, Cardiovascular Sciences, The Netherlands (J.P.v.T.).
  • Walsh R; Department of Genetics, UNC Chapel Hill, NC (J.G., C.T., E.W.C., S.B.C., J.M., L.V.M., B.A.S., N.S., K.W.).
  • Wells Q; National Heart and Lung Institute & MRC London Institute of Medical Sciences, Imperial College London, United Kingdom (R.W., N.W., J.S.W.).
  • Whiffin N; Cardiovascular Research Centre at Royal Brompton & Harefield Hospitals NHS Trust, London, United Kingdom (R.W., N.W., J.S.W.).
  • Witkowski L; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN (Q.W.).
  • Semsarian C; National Heart and Lung Institute & MRC London Institute of Medical Sciences, Imperial College London, United Kingdom (R.W., N.W., J.S.W.).
  • Ware JS; Cardiovascular Research Centre at Royal Brompton & Harefield Hospitals NHS Trust, London, United Kingdom (R.W., N.W., J.S.W.).
  • Hershberger RE; Department of Pathology, Harvard Medical School/Massachusetts General Hospital, Boston (L.W., B.F.).
  • Funke B; Agnes Ginges Centre for Molecular Cardiology at Centenary Institute and Faculty of Medicine and Health, The University of Sydney, University of Sydney, Australia (J.I., C.S.).
Circ Genom Precis Med ; 12(2): e002460, 2019 02.
Article in En | MEDLINE | ID: mdl-30681346
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Predisposition to Disease / Cardiomyopathy, Hypertrophic, Familial Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Circ Genom Precis Med Year: 2019 Type: Article
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Predisposition to Disease / Cardiomyopathy, Hypertrophic, Familial Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Circ Genom Precis Med Year: 2019 Type: Article