Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes.
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| Title: | Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes. |
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| Authors: | Rosenfeld JA; Signature Genomic Laboratories, Spokane, WA 99207, USA., Stephens LE, Coppinger J, Ballif BC, Hoo JJ, French BN, Banks VC, Smith WE, Manchester D, Tsai AC, Merrion K, Mendoza-Londono R, Dupuis L, Schultz R, Torchia B, Sahoo T, Bejjani B, Weaver DD, Shaffer LG |
| Source: | European journal of human genetics : EJHG [Eur J Hum Genet] 2011 May; Vol. 19 (5), pp. 547-54. Date of Electronic Publication: 2011 Jan 19. |
| Publication Type: | Journal Article |
| 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: 21248749 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Rosenfeld+JA%22">Rosenfeld JA</searchLink>; Signature Genomic Laboratories, Spokane, WA 99207, USA.<br /><searchLink fieldCode="AU" term="%22Stephens+LE%22">Stephens LE</searchLink><br /><searchLink fieldCode="AU" term="%22Coppinger+J%22">Coppinger J</searchLink><br /><searchLink fieldCode="AU" term="%22Ballif+BC%22">Ballif BC</searchLink><br /><searchLink fieldCode="AU" term="%22Hoo+JJ%22">Hoo JJ</searchLink><br /><searchLink fieldCode="AU" term="%22French+BN%22">French BN</searchLink><br /><searchLink fieldCode="AU" term="%22Banks+VC%22">Banks VC</searchLink><br /><searchLink fieldCode="AU" term="%22Smith+WE%22">Smith WE</searchLink><br /><searchLink fieldCode="AU" term="%22Manchester+D%22">Manchester D</searchLink><br /><searchLink fieldCode="AU" term="%22Tsai+AC%22">Tsai AC</searchLink><br /><searchLink fieldCode="AU" term="%22Merrion+K%22">Merrion K</searchLink><br /><searchLink fieldCode="AU" term="%22Mendoza-Londono+R%22">Mendoza-Londono R</searchLink><br /><searchLink fieldCode="AU" term="%22Dupuis+L%22">Dupuis L</searchLink><br /><searchLink fieldCode="AU" term="%22Schultz+R%22">Schultz R</searchLink><br /><searchLink fieldCode="AU" term="%22Torchia+B%22">Torchia B</searchLink><br /><searchLink fieldCode="AU" term="%22Sahoo+T%22">Sahoo T</searchLink><br /><searchLink fieldCode="AU" term="%22Bejjani+B%22">Bejjani B</searchLink><br /><searchLink fieldCode="AU" term="%22Weaver+DD%22">Weaver DD</searchLink><br /><searchLink fieldCode="AU" term="%22Shaffer+LG%22">Shaffer LG</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] 2011 May; Vol. 19 (5), pp. 547-54. <i>Date of Electronic Publication: </i>2011 Jan 19. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – 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=21248749 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/ejhg.2010.237 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 547 Titles: – TitleFull: Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Rosenfeld JA – PersonEntity: Name: NameFull: Stephens LE – PersonEntity: Name: NameFull: Coppinger J – PersonEntity: Name: NameFull: Ballif BC – PersonEntity: Name: NameFull: Hoo JJ – PersonEntity: Name: NameFull: French BN – PersonEntity: Name: NameFull: Banks VC – PersonEntity: Name: NameFull: Smith WE – PersonEntity: Name: NameFull: Manchester D – PersonEntity: Name: NameFull: Tsai AC – PersonEntity: Name: NameFull: Merrion K – PersonEntity: Name: NameFull: Mendoza-Londono R – PersonEntity: Name: NameFull: Dupuis L – PersonEntity: Name: NameFull: Schultz R – PersonEntity: Name: NameFull: Torchia B – PersonEntity: Name: NameFull: Sahoo T – PersonEntity: Name: NameFull: Bejjani B – PersonEntity: Name: NameFull: Weaver DD – PersonEntity: Name: NameFull: Shaffer LG IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 05 Text: 2011 May Type: published Y: 2011 Identifiers: – Type: issn-electronic Value: 1476-5438 Numbering: – Type: volume Value: 19 – Type: issue Value: 5 Titles: – TitleFull: European journal of human genetics : EJHG Type: main |
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