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Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variation.
Radford, Elizabeth J; Tan, Hong-Kee; Andersson, Malin H L; Stephenson, James D; Gardner, Eugene J; Ironfield, Holly; Waters, Andrew J; Gitterman, Daniel; Lindsay, Sarah; Abascal, Federico; Martincorena, Iñigo; Kolesnik-Taylor, Anna; Ng-Cordell, Elise; Firth, Helen V; Baker, Kate; Perry, John R B; Adams, David J; Gerety, Sebastian S; Hurles, Matthew E.
Afiliación
  • Radford EJ; Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
  • Tan HK; Department of Paediatrics, University of Cambridge, Level 8, Cambridge Biomedical Campus, Cambridge, CB2 0QQ, UK.
  • Andersson MHL; Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
  • Stephenson JD; Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
  • Gardner EJ; EMBL-EBI, Wellcome Genome Campus, Hinxton, CB10 1SD, UK.
  • Ironfield H; MRC Epidemiology Unit, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, CB2 0QQ, UK.
  • Waters AJ; Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
  • Gitterman D; Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
  • Lindsay S; Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
  • Abascal F; Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
  • Martincorena I; Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
  • Kolesnik-Taylor A; Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
  • Ng-Cordell E; MRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, UK.
  • Firth HV; MRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, UK.
  • Baker K; Department of Psychology, University of British Columbia, Vancouver, Canada.
  • Perry JRB; Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
  • Adams DJ; Department of Medical Genetics, University of Cambridge, Cambridge, UK.
  • Gerety SS; MRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, UK.
  • Hurles ME; Department of Medical Genetics, University of Cambridge, Cambridge, UK.
Nat Commun ; 14(1): 7702, 2023 Dec 06.
Article en En | MEDLINE | ID: mdl-38057330
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos del Neurodesarrollo / Neoplasias Límite: Female / Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos del Neurodesarrollo / Neoplasias Límite: Female / Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido