Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.
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| Title: | Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment. |
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| 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 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 26262844 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| 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 |
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