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Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes.
Bybjerg-Grauholm, Jonas; Hagen, Christian M; Gonçalves, Vanessa F; Bækvad-Hansen, Marie; Hansen, Christine S; Hedley, Paula L; Kanters, Jørgen K; Nielsen, Jimmi; Theisen, Michael; Mors, Ole; Kennedy, James; Als, Thomas D; Demur, Alfonso B; Nordentoft, Merete; Børglum, Anders; Mortensen, Preben B; Werge, Thomas M; Hougaard, David M; Christiansen, Michael.
Afiliação
  • Bybjerg-Grauholm J; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Hagen CM; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Gonçalves VF; Centre for Addiction and Mental Health, University of Toronto, Toronto, Canada.
  • Bækvad-Hansen M; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Hansen CS; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Hedley PL; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Kanters JK; Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Nielsen J; Aalborg Psychiatric Hospital. Aalborg University Hospital, Aalborg, Denmark.
  • Theisen M; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Mors O; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
  • Kennedy J; Centre for Addiction and Mental Health, University of Toronto, Toronto, Canada.
  • Als TD; Institute of Medical Genetics, Aarhus University, Aarhus, Denmark.
  • Demur AB; Mental Health Centre, Sct Hans, Capital Region of Denmark, Denmark.
  • Nordentoft M; Mental Health Centre, Capital Region of Denmark, Denmark.
  • Børglum A; Institute of Medical Genetics, Aarhus University, Aarhus, Denmark.
  • Mortensen PB; Center for Register Research, Institute of Economics, Aarhus University, Århus, Denmark.
  • Werge TM; Mental Health Centre, Sct Hans, Capital Region of Denmark, Denmark.
  • Hougaard DM; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Christiansen M; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
PLoS One ; 13(12): e0208829, 2018.
Article em En | MEDLINE | ID: mdl-30543675
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Haplótipos / DNA Mitocondrial / Polimorfismo de Nucleotídeo Único / População Branca Limite: Humans País/Região como assunto: Europa Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Dinamarca 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: Haplótipos / DNA Mitocondrial / Polimorfismo de Nucleotídeo Único / População Branca Limite: Humans País/Região como assunto: Europa Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Dinamarca País de publicação: Estados Unidos