Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
Saved in:
| Title: | Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair. |
|---|---|
| Authors: | 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. |
| Source: | Nature communications [Nat Commun] 2023 Jun 28; Vol. 14 (1), pp. 3836. Date of Electronic Publication: 2023 Jun 28. |
| Publication Type: | Published Erratum |
| Journal Info: | Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE; PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| FullText | Links: – Type: pdflink Text: Availability: 1 |
|---|---|
| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 37380644 AccessLevel: 2 PubTypeId: unknown PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Sherwood+K%22">Sherwood K</searchLink>; Cancer Research UK Edinburgh Centre and MRC Human Genetics Unit, Institute of Genomics and Cancer, Crewe Road, Edinburgh, EH4 2XU, UK.<br /><searchLink fieldCode="AU" term="%22Ward+JC%22">Ward JC</searchLink>; Dept of Oncology, University of Oxford, Old Road Campus Research Building, Roosevelt Drive, Oxford, OX3 7DQ, UK.<br /><searchLink fieldCode="AU" term="%22Soriano+I%22">Soriano I</searchLink>; Dept of Oncology, University of Oxford, Old Road Campus Research Building, Roosevelt Drive, Oxford, OX3 7DQ, UK.<br /><searchLink fieldCode="AU" term="%22Martin+L%22">Martin L</searchLink>; Institute of Cancer and Genomic Sciences, University of Birmingham Medical School, Vincent Drive, Edgbaston, Birmingham, B15 2JJ, UK.<br /><searchLink fieldCode="AU" term="%22Campbell+A%22">Campbell A</searchLink>; Centre for Genetics and Experimental Medicine, Institute of Genetics and Cancer, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.<br /><searchLink fieldCode="AU" term="%22Rahbari+R%22">Rahbari R</searchLink>; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.<br /><searchLink fieldCode="AU" term="%22Kafetzopoulos+I%22">Kafetzopoulos I</searchLink>; Cancer Research UK Edinburgh Centre and MRC Human Genetics Unit, Institute of Genomics and Cancer, Crewe Road, Edinburgh, EH4 2XU, UK.<br /><searchLink fieldCode="AU" term="%22Sproul+D%22">Sproul D</searchLink>; Cancer Research UK Edinburgh Centre and MRC Human Genetics Unit, Institute of Genomics and Cancer, Crewe Road, Edinburgh, EH4 2XU, UK.<br /><searchLink fieldCode="AU" term="%22Green+A%22">Green A</searchLink>; Department of Clinical Genetics, Children's Health Ireland and School of Medicine University College, Dublin, Ireland.<br /><searchLink fieldCode="AU" term="%22Sampson+JR%22">Sampson JR</searchLink>; Institute of Medical Genetics, Division of Cancer and Genetics, Cardiff University School of Medicine, Cardiff, UK.<br /><searchLink fieldCode="AU" term="%22Donaldson+A%22">Donaldson A</searchLink>; Bristol Regional Clinical Genetics Service, St Michael's Hospital, Southwell Street, Bristol, BS2 8EG, UK.<br /><searchLink fieldCode="AU" term="%22Ong+KR%22">Ong KR</searchLink>; West Midlands Regional Genetics Service, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.<br /><searchLink fieldCode="AU" term="%22Heinimann+K%22">Heinimann K</searchLink>; Institute for Medical Genetics and Pathology, University Hospital Basel, Basel, BS, Switzerland.<br /><searchLink fieldCode="AU" term="%22Nielsen+M%22">Nielsen M</searchLink>; Department of Clinical Genetics, Leiden University Medical Centre, 2333 ZA, Leiden, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Thomas+H%22">Thomas H</searchLink>; St Mark's Hospital, Watford Road, Harrow, HA1 3UJ, UK.<br /><searchLink fieldCode="AU" term="%22Latchford+A%22">Latchford A</searchLink>; St Mark's Hospital, Watford Road, Harrow, HA1 3UJ, UK.<br /><searchLink fieldCode="AU" term="%22Palles+C%22">Palles C</searchLink>; Institute of Cancer and Genomic Sciences, University of Birmingham Medical School, Vincent Drive, Edgbaston, Birmingham, B15 2JJ, UK. c.palles@bham.ac.uk.<br /><searchLink fieldCode="AU" term="%22Tomlinson+I%22">Tomlinson I</searchLink>; Dept of Oncology, University of Oxford, Old Road Campus Research Building, Roosevelt Drive, Oxford, OX3 7DQ, UK. ian.tomlinson@oncology.ox.ac.uk. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101528555%22">Nature communications</searchLink> [Nat Commun] 2023 Jun 28; Vol. 14 (1), pp. 3836. <i>Date of Electronic Publication: </i>2023 Jun 28. – Name: TypePub Label: Publication Type Group: TypPub Data: Published Erratum – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Pub%2E+Group%22">Nature Pub. Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101528555 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2041-1723 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2220411723%22">20411723 </searchLink><i>NLM ISO Abbreviation: </i>Nat Commun <i>Subsets: </i>MEDLINE; PubMed not MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=37380644 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/s41467-023-39587-y Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 3836 Titles: – TitleFull: Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Sherwood K – PersonEntity: Name: NameFull: Ward JC – PersonEntity: Name: NameFull: Soriano I – PersonEntity: Name: NameFull: Martin L – PersonEntity: Name: NameFull: Campbell A – PersonEntity: Name: NameFull: Rahbari R – PersonEntity: Name: NameFull: Kafetzopoulos I – PersonEntity: Name: NameFull: Sproul D – PersonEntity: Name: NameFull: Green A – PersonEntity: Name: NameFull: Sampson JR – PersonEntity: Name: NameFull: Donaldson A – PersonEntity: Name: NameFull: Ong KR – PersonEntity: Name: NameFull: Heinimann K – PersonEntity: Name: NameFull: Nielsen M – PersonEntity: Name: NameFull: Thomas H – PersonEntity: Name: NameFull: Latchford A – PersonEntity: Name: NameFull: Palles C – PersonEntity: Name: NameFull: Tomlinson I IsPartOfRelationships: – BibEntity: Dates: – D: 28 M: 06 Text: 2023 Jun 28 Type: published Y: 2023 Identifiers: – Type: issn-electronic Value: 2041-1723 Numbering: – Type: volume Value: 14 – Type: issue Value: 1 Titles: – TitleFull: Nature communications Type: main |
| ResultId | 1 |