Your browser doesn't support javascript.
loading
NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversity.
Abou Hassan, Ossama K; Fahed, Akl C; Batrawi, Manal; Arabi, Mariam; Refaat, Marwan M; DePalma, Steven R; Seidman, J G; Seidman, Christine E; Bitar, Fadi F; Nemer, Georges M.
Afiliação
  • Abou Hassan OK; 1] Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon [2] Department of Internal Medicine, American University of Beirut, Beirut, Lebanon.
  • Fahed AC; 1] Department of Genetics, Harvard Medical School, Boston, MA [2] Department of Medicine, Massachusetts General Hospital, Boston, MA.
  • Batrawi M; Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon.
  • Arabi M; Department of Pediatrics and Adolescent Medicine, American University of Beirut, Beirut, Lebanon.
  • Refaat MM; 1] Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon [2] Department of Internal Medicine, American University of Beirut, Beirut, Lebanon.
  • DePalma SR; Department of Genetics, Harvard Medical School, Boston, MA.
  • Seidman JG; Department of Genetics, Harvard Medical School, Boston, MA.
  • Seidman CE; 1] Department of Genetics, Harvard Medical School, Boston, MA [2] Howard Hughes Medical Institute and Division of Cardiology, Brigham and Women's Hospital, Boston, MA.
  • Bitar FF; 1] Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon [2] Department of Pediatrics and Adolescent Medicine, American University of Beirut, Beirut, Lebanon.
  • Nemer GM; Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon.
Sci Rep ; 5: 8848, 2015 Mar 06.
Article em En | MEDLINE | ID: mdl-25742962
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Proteínas de Homeodomínio / Consanguinidade / Cardiopatias Congênitas / Mutação Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Proteínas de Homeodomínio / Consanguinidade / Cardiopatias Congênitas / Mutação Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2015 Tipo de documento: Article