Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders.
Saved in:
| Title: | Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders. |
|---|---|
| Authors: | Boccuto L; Greenwood Genetic Center, Greenwood, SC, USA., Lauri M, Sarasua SM, Skinner CD, Buccella D, Dwivedi A, Orteschi D, Collins JS, Zollino M, Visconti P, Dupont B, Tiziano D, Schroer RJ, Neri G, Stevenson RE, Gurrieri F, Schwartz CE |
| Source: | European journal of human genetics : EJHG [Eur J Hum Genet] 2013 Mar; Vol. 21 (3), pp. 310-6. Date of Electronic Publication: 2012 Aug 15. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| 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: 22892527 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Boccuto+L%22">Boccuto L</searchLink>; Greenwood Genetic Center, Greenwood, SC, USA.<br /><searchLink fieldCode="AU" term="%22Lauri+M%22">Lauri M</searchLink><br /><searchLink fieldCode="AU" term="%22Sarasua+SM%22">Sarasua SM</searchLink><br /><searchLink fieldCode="AU" term="%22Skinner+CD%22">Skinner CD</searchLink><br /><searchLink fieldCode="AU" term="%22Buccella+D%22">Buccella D</searchLink><br /><searchLink fieldCode="AU" term="%22Dwivedi+A%22">Dwivedi A</searchLink><br /><searchLink fieldCode="AU" term="%22Orteschi+D%22">Orteschi D</searchLink><br /><searchLink fieldCode="AU" term="%22Collins+JS%22">Collins JS</searchLink><br /><searchLink fieldCode="AU" term="%22Zollino+M%22">Zollino M</searchLink><br /><searchLink fieldCode="AU" term="%22Visconti+P%22">Visconti P</searchLink><br /><searchLink fieldCode="AU" term="%22Dupont+B%22">Dupont B</searchLink><br /><searchLink fieldCode="AU" term="%22Tiziano+D%22">Tiziano D</searchLink><br /><searchLink fieldCode="AU" term="%22Schroer+RJ%22">Schroer RJ</searchLink><br /><searchLink fieldCode="AU" term="%22Neri+G%22">Neri G</searchLink><br /><searchLink fieldCode="AU" term="%22Stevenson+RE%22">Stevenson RE</searchLink><br /><searchLink fieldCode="AU" term="%22Gurrieri+F%22">Gurrieri F</searchLink><br /><searchLink fieldCode="AU" term="%22Schwartz+CE%22">Schwartz CE</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] 2013 Mar; Vol. 21 (3), pp. 310-6. <i>Date of Electronic Publication: </i>2012 Aug 15. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't – 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=22892527 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/ejhg.2012.175 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 310 Titles: – TitleFull: Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Boccuto L – PersonEntity: Name: NameFull: Lauri M – PersonEntity: Name: NameFull: Sarasua SM – PersonEntity: Name: NameFull: Skinner CD – PersonEntity: Name: NameFull: Buccella D – PersonEntity: Name: NameFull: Dwivedi A – PersonEntity: Name: NameFull: Orteschi D – PersonEntity: Name: NameFull: Collins JS – PersonEntity: Name: NameFull: Zollino M – PersonEntity: Name: NameFull: Visconti P – PersonEntity: Name: NameFull: Dupont B – PersonEntity: Name: NameFull: Tiziano D – PersonEntity: Name: NameFull: Schroer RJ – PersonEntity: Name: NameFull: Neri G – PersonEntity: Name: NameFull: Stevenson RE – PersonEntity: Name: NameFull: Gurrieri F – PersonEntity: Name: NameFull: Schwartz CE IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: 2013 Mar Type: published Y: 2013 Identifiers: – Type: issn-electronic Value: 1476-5438 Numbering: – Type: volume Value: 21 – Type: issue Value: 3 Titles: – TitleFull: European journal of human genetics : EJHG Type: main |
| ResultId | 1 |