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Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.
Tester, David J; Wong, Leonie C H; Chanana, Pritha; Gray, Belinda; Jaye, Amie; Evans, Jared M; Evans, Margaret; Fleming, Peter; Jeffrey, Iona; Cohen, Marta; Tfelt-Hansen, Jacob; Simpson, Michael A; Behr, Elijah R; Ackerman, Michael J.
Afiliação
  • Tester DJ; Department of Cardiovascular Medicine (Division of Heart Rhythm Services), Pediatrics (Division of Pediatric Cardiology), Molecular Pharmacology & Experimental Therapeutics (Windland Smith Rice Sudden Death Genomics Laboratory), Mayo Clinic, Rochester, MN.
  • Wong LCH; Molecular and Clinical Sciences Research Institute, St George's University of London, London, United Kingdom; Cardiology Clinical Academic Group, St George's University Hospitals' National Health Service (NHS) Foundation Trust, London, United Kingdom.
  • Chanana P; Department of Health Sciences Research, Mayo Clinic, Rochester, MN.
  • Gray B; Molecular and Clinical Sciences Research Institute, St George's University of London, London, United Kingdom; Cardiology Clinical Academic Group, St George's University Hospitals' National Health Service (NHS) Foundation Trust, London, United Kingdom; Agnes Ginges Centre for Molecular Cardiology, Ce
  • Jaye A; Medical and Molecular Genetics, Guy's Hospital, King's College London, London, United Kingdom.
  • Evans JM; Department of Health Sciences Research, Mayo Clinic, Rochester, MN.
  • Evans M; Department of Pathology, Royal Infirmary of Edinburgh, Edinburgh, United Kingdom.
  • Fleming P; Centre for Child and Adolescent Health, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
  • Jeffrey I; Department of Cellular Pathology, St George's University of London, London, United Kingdom; Department of Cellular Pathology, St George's University Hospitals NHS Foundation Trust, London, United Kingdom.
  • Cohen M; Histopathology Department, Sheffield Children's Hospital NHS FT, Sheffield, United Kingdom.
  • Tfelt-Hansen J; Department of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark; Department of Forensic Medicine, Faculty of Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Simpson MA; Medical and Molecular Genetics, Guy's Hospital, King's College London, London, United Kingdom.
  • Behr ER; Molecular and Clinical Sciences Research Institute, St George's University of London, London, United Kingdom; Cardiology Clinical Academic Group, St George's University Hospitals' National Health Service (NHS) Foundation Trust, London, United Kingdom.
  • Ackerman MJ; Department of Cardiovascular Medicine (Division of Heart Rhythm Services), Pediatrics (Division of Pediatric Cardiology), Molecular Pharmacology & Experimental Therapeutics (Windland Smith Rice Sudden Death Genomics Laboratory), Mayo Clinic, Rochester, MN. Electronic address: ackerman.michael@ma
J Pediatr ; 203: 423-428.e11, 2018 12.
Article em En | MEDLINE | ID: mdl-30268395
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Morte Súbita do Lactente / Predisposição Genética para Doença / Exoma Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: America do norte / Europa Idioma: En Revista: J Pediatr Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Mongólia
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Morte Súbita do Lactente / Predisposição Genética para Doença / Exoma Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: America do norte / Europa Idioma: En Revista: J Pediatr Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Mongólia