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Author Correction: Clinically-relevant postzygotic mosaicism in parents and children with developmental disorders in trio exome sequencing data.
Wright, C F; Prigmore, E; Rajan, D; Handsaker, J; McRae, J; Kaplanis, J; Fitzgerald, T W; FitzPatrick, D R; Firth, H V; Hurles, M E.
Afiliação
  • Wright CF; Institute of Biomedicine and Clinical Science, College of Medicine and Health, University of Exeter, RILD Building, Royal Devon and Exeter Hospital, Exeter, EX2 5DW, UK. caroline.wright@exeter.ac.uk.
  • Prigmore E; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.
  • Rajan D; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.
  • Handsaker J; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.
  • McRae J; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.
  • Kaplanis J; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.
  • Fitzgerald TW; European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Cambridge, CB10 1SD, UK.
  • FitzPatrick DR; MRC Human Genetics Unit, University of Edinburgh, Edinburgh, EH4 2XU, UK.
  • Firth HV; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.
  • Hurles ME; Clinical Genetics, Box 134 Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.
Nat Commun ; 13(1): 5674, 2022 Sep 27.
Article em En | MEDLINE | ID: mdl-36167847

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article