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Association of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History.
Patel, Aniruddh P; Wang, Minxian; Fahed, Akl C; Mason-Suares, Heather; Brockman, Deanna; Pelletier, Renee; Amr, Sami; Machini, Kalotina; Hawley, Megan; Witkowski, Leora; Koch, Christopher; Philippakis, Anthony; Cassa, Christopher A; Ellinor, Patrick T; Kathiresan, Sekar; Ng, Kenney; Lebo, Matthew; Khera, Amit V.
Afiliação
  • Patel AP; Division of Cardiology and Center for Genomic Medicine, Department of Medicine, Massachusetts General Hospital, Boston.
  • Wang M; Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Fahed AC; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
  • Mason-Suares H; Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Brockman D; Division of Cardiology and Center for Genomic Medicine, Department of Medicine, Massachusetts General Hospital, Boston.
  • Pelletier R; Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Amr S; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
  • Machini K; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
  • Hawley M; Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, Boston, Massachusetts.
  • Witkowski L; Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
  • Koch C; Division of Cardiology and Center for Genomic Medicine, Department of Medicine, Massachusetts General Hospital, Boston.
  • Philippakis A; Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Cassa CA; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
  • Ellinor PT; Division of Cardiology and Center for Genomic Medicine, Department of Medicine, Massachusetts General Hospital, Boston.
  • Kathiresan S; Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Ng K; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
  • Lebo M; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
  • Khera AV; Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, Boston, Massachusetts.
JAMA Netw Open ; 3(4): e203959, 2020 04 01.
Article em En | MEDLINE | ID: mdl-32347951
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Predisposição Genética para Doença / Síndrome Hereditária de Câncer de Mama e Ovário / Hiperlipoproteinemia Tipo II Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: JAMA Netw Open Ano de publicação: 2020 Tipo de documento: Article País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Predisposição Genética para Doença / Síndrome Hereditária de Câncer de Mama e Ovário / Hiperlipoproteinemia Tipo II Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: JAMA Netw Open Ano de publicação: 2020 Tipo de documento: Article País de publicação: Estados Unidos