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De novo mutations in autosomal recessive congenital malformations.
Black, Holly A; Parry, David; Atanur, Santosh S; Ross, David; Rose, Elaine; Russell, Helen; Stock, Sarah; Warner, Jon; Porteous, Mary; Aitman, Timothy J; Evans, Margaret J.
Afiliação
  • Black HA; Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Parry D; Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Atanur SS; Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Ross D; Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Rose E; Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Russell H; NHS Fife Fetal Medicine Unit, Victoria Hospital, Kirkcaldy, UK.
  • Stock S; Tommy's Centre for Maternal and Fetal Health, MRC University of Edinburgh Centre for Reproductive Health, The Queen's Medical Research Institute, Edinburgh, UK.
  • Warner J; South East of Scotland Clinical Genetics Service, Western General Hospital, Edinburgh, UK.
  • Porteous M; South East of Scotland Clinical Genetics Service, Western General Hospital, Edinburgh, UK.
  • Aitman TJ; Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Evans MJ; Department of Pathology, NHS Lothian, Edinburgh, UK.
Genet Med ; 18(12): 1325-1326, 2016 12.
Article em En | MEDLINE | ID: mdl-27280866
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linhagem / Genes Recessivos Limite: Humans Idioma: En Revista: Genet Med Ano de publicação: 2016 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: Linhagem / Genes Recessivos Limite: Humans Idioma: En Revista: Genet Med Ano de publicação: 2016 Tipo de documento: Article