Your browser doesn't support javascript.
loading
Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
Sherwood, Kitty; Ward, Joseph C; Soriano, Ignacio; Martin, Lynn; Campbell, Archie; Rahbari, Raheleh; Kafetzopoulos, Ioannis; Sproul, Duncan; Green, Andrew; Sampson, Julian R; Donaldson, Alan; Ong, Kai-Ren; Heinimann, Karl; Nielsen, Maartje; Thomas, Huw; Latchford, Andrew; Palles, Claire; Tomlinson, Ian.
Afiliação
  • Sherwood K; Cancer Research UK Edinburgh Centre and MRC Human Genetics Unit, Institute of Genomics and Cancer, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Ward JC; Dept of Oncology, University of Oxford, Old Road Campus Research Building, Roosevelt Drive, Oxford, OX3 7DQ, UK.
  • Soriano I; Dept of Oncology, University of Oxford, Old Road Campus Research Building, Roosevelt Drive, Oxford, OX3 7DQ, UK.
  • Martin L; Institute of Cancer and Genomic Sciences, University of Birmingham Medical School, Vincent Drive, Edgbaston, Birmingham, B15 2JJ, UK.
  • Campbell A; Centre for Genetics and Experimental Medicine, Institute of Genetics and Cancer, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Rahbari R; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Kafetzopoulos I; Cancer Research UK Edinburgh Centre and MRC Human Genetics Unit, Institute of Genomics and Cancer, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Sproul D; Cancer Research UK Edinburgh Centre and MRC Human Genetics Unit, Institute of Genomics and Cancer, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Green A; Department of Clinical Genetics, Children's Health Ireland and School of Medicine University College, Dublin, Ireland.
  • Sampson JR; Institute of Medical Genetics, Division of Cancer and Genetics, Cardiff University School of Medicine, Cardiff, UK.
  • Donaldson A; Bristol Regional Clinical Genetics Service, St Michael's Hospital, Southwell Street, Bristol, BS2 8EG, UK.
  • Ong KR; West Midlands Regional Genetics Service, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.
  • Heinimann K; Institute for Medical Genetics and Pathology, University Hospital Basel, Basel, BS, Switzerland.
  • Nielsen M; Department of Clinical Genetics, Leiden University Medical Centre, 2333 ZA, Leiden, the Netherlands.
  • Thomas H; St Mark's Hospital, Watford Road, Harrow, HA1 3UJ, UK.
  • Latchford A; St Mark's Hospital, Watford Road, Harrow, HA1 3UJ, UK.
  • Palles C; Institute of Cancer and Genomic Sciences, University of Birmingham Medical School, Vincent Drive, Edgbaston, Birmingham, B15 2JJ, UK. c.palles@bham.ac.uk.
  • Tomlinson I; Dept of Oncology, University of Oxford, Old Road Campus Research Building, Roosevelt Drive, Oxford, OX3 7DQ, UK. ian.tomlinson@oncology.ox.ac.uk.
Nat Commun ; 14(1): 3836, 2023 Jun 28.
Article em En | MEDLINE | ID: mdl-37380644

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article