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Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy.
Bagnall, Richard D; Ingles, Jodie; Dinger, Marcel E; Cowley, Mark J; Ross, Samantha Barratt; Minoche, André E; Lal, Sean; Turner, Christian; Colley, Alison; Rajagopalan, Sulekha; Berman, Yemima; Ronan, Anne; Fatkin, Diane; Semsarian, Christopher.
Afiliação
  • Bagnall RD; Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Sydney, New South Wales, Australia; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Ingles J; Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Sydney, New South Wales, Australia; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.
  • Dinger ME; Garvan Institute of Medical Research, Sydney, New South Wales, Australia; St. Vincent's Hospital Clinical School, University of New South Wales, Sydney, New South Wales, Australia.
  • Cowley MJ; Garvan Institute of Medical Research, Sydney, New South Wales, Australia; St. Vincent's Hospital Clinical School, University of New South Wales, Sydney, New South Wales, Australia.
  • Ross SB; Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Sydney, New South Wales, Australia; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Minoche AE; Garvan Institute of Medical Research, Sydney, New South Wales, Australia.
  • Lal S; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.
  • Turner C; The Sydney Children's Hospital, Westmead, New South Wales, Australia.
  • Colley A; Department of Clinical Genetics, Liverpool Hospital, Liverpool, New South Wales, Australia.
  • Rajagopalan S; Department of Clinical Genetics, Liverpool Hospital, Liverpool, New South Wales, Australia.
  • Berman Y; Clinical Genetics Department, Royal North Shore Hospital, Sydney, New South Wales, Australia.
  • Ronan A; Hunter Genetics Unit, Newcastle, New South Wales, Australia; University of Newcastle, Newcastle, New South Wales, Australia.
  • Fatkin D; St. Vincent's Hospital Clinical School, University of New South Wales, Sydney, New South Wales, Australia; Molecular Cardiology and Biophysics Division, Victor Chang Cardiac Research Institute, Sydney, New South Wales, Australia; Cardiology Department, St. Vincent's Hospital, Sydney, New South Wales
  • Semsarian C; Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Sydney, New South Wales, Australia; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia. Electronic address: c.se
J Am Coll Cardiol ; 72(4): 419-429, 2018 07 24.
Article em En | MEDLINE | ID: mdl-30025578
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cardiomiopatia Hipertrófica / Sequenciamento Completo do Genoma Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Oceania Idioma: En Revista: J Am Coll Cardiol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Austrália
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cardiomiopatia Hipertrófica / Sequenciamento Completo do Genoma Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Oceania Idioma: En Revista: J Am Coll Cardiol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Austrália