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A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants.
Nedeljkovic, Ivana; Terzikhan, Natalie; Vonk, Judith M; van der Plaat, Diana A; Lahousse, Lies; van Diemen, Cleo C; Hobbs, Brian D; Qiao, Dandi; Cho, Michael H; Brusselle, Guy G; Postma, Dirkje S; Boezen, H M; van Duijn, Cornelia M; Amin, Najaf.
Afiliação
  • Nedeljkovic I; Department of Epidemiology, Erasmus Medical Center, Rotterdam, Netherlands.
  • Terzikhan N; Department of Epidemiology, Erasmus Medical Center, Rotterdam, Netherlands.
  • Vonk JM; Department of Respiratory Medicine, Ghent University Hospital, Ghent, Belgium.
  • van der Plaat DA; Department of Epidemiology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
  • Lahousse L; Groningen Research Institute for Asthma and COPD, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
  • van Diemen CC; Department of Epidemiology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
  • Hobbs BD; Groningen Research Institute for Asthma and COPD, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
  • Qiao D; Department of Epidemiology, Erasmus Medical Center, Rotterdam, Netherlands.
  • Cho MH; Department of Respiratory Medicine, Ghent University Hospital, Ghent, Belgium.
  • Brusselle GG; Pharmaceutical Care Unit, Department of Bioanalysis, Ghent University, Ghent, Belgium.
  • Postma DS; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
  • Boezen HM; Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, United States.
  • van Duijn CM; Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Boston, MA, United States.
  • Amin N; Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, United States.
Front Genet ; 9: 133, 2018.
Article em En | MEDLINE | ID: mdl-29725345
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Systematic_reviews Idioma: En Revista: Front Genet Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Holanda País de publicação: Suíça
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Systematic_reviews Idioma: En Revista: Front Genet Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Holanda País de publicação: Suíça