Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.

Saved in:
Bibliographic Details
Title: Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.
Authors: Pettigrew KA; School of Medicine, University of St Andrews, St Andrews, United Kingdom., Reeves E; Department of Psychology, University of York, York, United Kingdom., Leavett R; Department of Psychology, University of York, York, United Kingdom., Hayiou-Thomas ME; Department of Psychology, University of York, York, United Kingdom., Sharma A; School of Medicine, University of St Andrews, St Andrews, United Kingdom., Simpson NH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom., Martinelli A; School of Medicine, University of St Andrews, St Andrews, United Kingdom., Thompson P; Department of Experimental Psychology, University of Oxford, Oxford, United Kingdom., Hulme C; Division of Psychology and Language Sciences, University College London, London, United Kingdom., Snowling MJ; Department of Experimental Psychology, University of Oxford, Oxford, United Kingdom; St. Johns College, University of Oxford, Oxford, United Kingdom., Newbury DF; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom., Paracchini S; School of Medicine, University of St Andrews, St Andrews, United Kingdom.
Source: PloS one [PLoS One] 2015 Aug 11; Vol. 10 (8), pp. e0134997. Date of Electronic Publication: 2015 Aug 11 (Print Publication: 2015).
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
Database: MEDLINE Ultimate
FullText Links:
  – Type: pdflink
Text:
  Availability: 0
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 26262844
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Pettigrew+KA%22">Pettigrew KA</searchLink>; School of Medicine, University of St Andrews, St Andrews, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Reeves+E%22">Reeves E</searchLink>; Department of Psychology, University of York, York, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Leavett+R%22">Leavett R</searchLink>; Department of Psychology, University of York, York, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Hayiou-Thomas+ME%22">Hayiou-Thomas ME</searchLink>; Department of Psychology, University of York, York, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Sharma+A%22">Sharma A</searchLink>; School of Medicine, University of St Andrews, St Andrews, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Simpson+NH%22">Simpson NH</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Martinelli+A%22">Martinelli A</searchLink>; School of Medicine, University of St Andrews, St Andrews, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Thompson+P%22">Thompson P</searchLink>; Department of Experimental Psychology, University of Oxford, Oxford, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Hulme+C%22">Hulme C</searchLink>; Division of Psychology and Language Sciences, University College London, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Snowling+MJ%22">Snowling MJ</searchLink>; Department of Experimental Psychology, University of Oxford, Oxford, United Kingdom; St. Johns College, University of Oxford, Oxford, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Newbury+DF%22">Newbury DF</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Paracchini+S%22">Paracchini S</searchLink>; School of Medicine, University of St Andrews, St Andrews, United Kingdom.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22101285081%22">PloS one</searchLink> [PLoS One] 2015 Aug 11; Vol. 10 (8), pp. e0134997. <i>Date of Electronic Publication: </i>2015 Aug 11 (<i>Print Publication: </i>2015).
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article; Research Support, Non-U.S. Gov't
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Public+Library+of+Science%22">Public Library of Science </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101285081 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>1932-6203 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2219326203%22">19326203 </searchLink><i>NLM ISO Abbreviation: </i>PLoS One <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=26262844
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1371/journal.pone.0134997
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: e0134997
    Titles:
      – TitleFull: Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Pettigrew KA
      – PersonEntity:
          Name:
            NameFull: Reeves E
      – PersonEntity:
          Name:
            NameFull: Leavett R
      – PersonEntity:
          Name:
            NameFull: Hayiou-Thomas ME
      – PersonEntity:
          Name:
            NameFull: Sharma A
      – PersonEntity:
          Name:
            NameFull: Simpson NH
      – PersonEntity:
          Name:
            NameFull: Martinelli A
      – PersonEntity:
          Name:
            NameFull: Thompson P
      – PersonEntity:
          Name:
            NameFull: Hulme C
      – PersonEntity:
          Name:
            NameFull: Snowling MJ
      – PersonEntity:
          Name:
            NameFull: Newbury DF
      – PersonEntity:
          Name:
            NameFull: Paracchini S
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 11
              M: 08
              Text: 2015 Aug 11
              Type: published
              Y: 2015
          Identifiers:
            – Type: issn-electronic
              Value: 1932-6203
          Numbering:
            – Type: volume
              Value: 10
            – Type: issue
              Value: 8
          Titles:
            – TitleFull: PloS one
              Type: main
ResultId 1