Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'.

Saved in:
Bibliographic Details
Title: Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'.
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
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 25537359
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
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
ResultId 1