Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'.
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| Title: | Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'. |
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| Authors: | Ceroni F; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Simpson NH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Francks C; 1] Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands [2] Donders Institute for Brain, Cognition & Behaviour, Nijmegen, The Netherlands., Baird G; Guy's & St Thomas NHS Foundation Trust, Newcomen Children's Neurosciences Centre, St Thomas' Hospital, London, UK., Conti-Ramsden G; School of Psychological Sciences, The University of Manchester, Manchester, UK., Clark A; Speech and Hearing Sciences, Queen Margaret University, Edinburgh, UK., Bolton PF; Departments of Child & Adolescent Psychiatry & Social Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Kings College London, London, UK., Hennessy ER; University Child Health and DMDE, University of Aberdeen, Aberdeen, UK., Donnelly P; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Bentley DR; Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex, UK., Martin H; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Parr J; Institute of Neuroscience and Health and Society, Newcastle University, Newcastle upon Tyne, UK., Pagnamenta AT; 1] Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK [2] NIHR Biomedical Research Centre, Oxford and Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Maestrini E; Dipartimento di Farmacia e Biotecnologie, University of Bologna, Bologna, Italy., Bacchelli E; Dipartimento di Farmacia e Biotecnologie, University of Bologna, Bologna, Italy., Fisher SE; 1] Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands [2] Donders Institute for Brain, Cognition & Behaviour, Nijmegen, The Netherlands., Newbury DF; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK. |
| Corporate Authors: | IMGSAC, SLI Consortium, WGS500 Consortium |
| Source: | European journal of human genetics : EJHG [Eur J Hum Genet] 2015 Sep; Vol. 23 (9), pp. 1113-5. Date of Electronic Publication: 2014 Dec 24. |
| Publication Type: | Journal Article; Comment |
| Journal Info: | Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 25537359 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Ceroni+F%22">Ceroni F</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Simpson+NH%22">Simpson NH</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Francks+C%22">Francks C</searchLink>; 1] Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands [2] Donders Institute for Brain, Cognition & Behaviour, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Baird+G%22">Baird G</searchLink>; Guy's & St Thomas NHS Foundation Trust, Newcomen Children's Neurosciences Centre, St Thomas' Hospital, London, UK.<br /><searchLink fieldCode="AU" term="%22Conti-Ramsden+G%22">Conti-Ramsden G</searchLink>; School of Psychological Sciences, The University of Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Clark+A%22">Clark A</searchLink>; Speech and Hearing Sciences, Queen Margaret University, Edinburgh, UK.<br /><searchLink fieldCode="AU" term="%22Bolton+PF%22">Bolton PF</searchLink>; Departments of Child & Adolescent Psychiatry & Social Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Kings College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Hennessy+ER%22">Hennessy ER</searchLink>; University Child Health and DMDE, University of Aberdeen, Aberdeen, UK.<br /><searchLink fieldCode="AU" term="%22Donnelly+P%22">Donnelly P</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Bentley+DR%22">Bentley DR</searchLink>; Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex, UK.<br /><searchLink fieldCode="AU" term="%22Martin+H%22">Martin H</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Parr+J%22">Parr J</searchLink>; Institute of Neuroscience and Health and Society, Newcastle University, Newcastle upon Tyne, UK.<br /><searchLink fieldCode="AU" term="%22Pagnamenta+AT%22">Pagnamenta AT</searchLink>; 1] Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK [2] NIHR Biomedical Research Centre, Oxford and Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Maestrini+E%22">Maestrini E</searchLink>; Dipartimento di Farmacia e Biotecnologie, University of Bologna, Bologna, Italy.<br /><searchLink fieldCode="AU" term="%22Bacchelli+E%22">Bacchelli E</searchLink>; Dipartimento di Farmacia e Biotecnologie, University of Bologna, Bologna, Italy.<br /><searchLink fieldCode="AU" term="%22Fisher+SE%22">Fisher SE</searchLink>; 1] Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands [2] Donders Institute for Brain, Cognition & Behaviour, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Newbury+DF%22">Newbury DF</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK. – Name: AuthorCorporate Label: Corporate Authors Group: Au Data: <searchLink fieldCode="CA" term="%22IMGSAC%22">IMGSAC</searchLink><br /><searchLink fieldCode="CA" term="%22SLI+Consortium%22">SLI Consortium</searchLink><br /><searchLink fieldCode="CA" term="%22WGS500+Consortium%22">WGS500 Consortium</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229302235%22">European journal of human genetics : EJHG</searchLink> [Eur J Hum Genet] 2015 Sep; Vol. 23 (9), pp. 1113-5. <i>Date of Electronic Publication: </i>2014 Dec 24. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Comment – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Publishing+Group%22">Nature Publishing Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9302235 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1476-5438 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210184813%22">10184813 </searchLink><i>NLM ISO Abbreviation: </i>Eur J Hum Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=25537359 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/ejhg.2014.275 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1113 Titles: – TitleFull: Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ceroni F – PersonEntity: Name: NameFull: Simpson NH – PersonEntity: Name: NameFull: Francks C – PersonEntity: Name: NameFull: Baird G – PersonEntity: Name: NameFull: Conti-Ramsden G – PersonEntity: Name: NameFull: Clark A – PersonEntity: Name: NameFull: Bolton PF – PersonEntity: Name: NameFull: Hennessy ER – PersonEntity: Name: NameFull: Donnelly P – PersonEntity: Name: NameFull: Bentley DR – PersonEntity: Name: NameFull: Martin H – PersonEntity: Name: NameFull: Parr J – PersonEntity: Name: NameFull: Pagnamenta AT – PersonEntity: Name: NameFull: Maestrini E – PersonEntity: Name: NameFull: Bacchelli E – PersonEntity: Name: NameFull: Fisher SE – PersonEntity: Name: NameFull: Newbury DF IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 09 Text: 2015 Sep Type: published Y: 2015 Identifiers: – Type: issn-electronic Value: 1476-5438 Numbering: – Type: volume Value: 23 – Type: issue Value: 9 Titles: – TitleFull: European journal of human genetics : EJHG Type: main |
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