18q- chromosomal abnormality in a phenotypically normal 2 1/2-year-old male with autism.
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| Title: | 18q- chromosomal abnormality in a phenotypically normal 2 1/2-year-old male with autism. |
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| Authors: | Seshadri K; Robert Wood Johnson Medical School, New Brunswick, NJ 08903-0019., Wallerstein R, Burack G |
| Source: | Developmental medicine and child neurology [Dev Med Child Neurol] 1992 Nov; Vol. 34 (11), pp. 1005-9. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: Blackwell Country of Publication: England NLM ID: 0006761 Publication Model: Print Cited Medium: Print ISSN: 0012-1622 (Print) Linking ISSN: 00121622 NLM ISO Abbreviation: Dev Med Child Neurol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 1426678 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: 18q- chromosomal abnormality in a phenotypically normal 2 1/2-year-old male with autism. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Seshadri+K%22">Seshadri K</searchLink>; Robert Wood Johnson Medical School, New Brunswick, NJ 08903-0019.<br /><searchLink fieldCode="AU" term="%22Wallerstein+R%22">Wallerstein R</searchLink><br /><searchLink fieldCode="AU" term="%22Burack+G%22">Burack G</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220006761%22">Developmental medicine and child neurology</searchLink> [Dev Med Child Neurol] 1992 Nov; Vol. 34 (11), pp. 1005-9. – Name: TypePub Label: Publication Type Group: TypPub Data: Case Reports; Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Blackwell%22">Blackwell </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>0006761 <i>Publication Model: </i>Print <i>Cited Medium: </i>Print <i>ISSN: </i>0012-1622 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200121622%22">00121622 </searchLink><i>NLM ISO Abbreviation: </i>Dev Med Child Neurol <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=1426678 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/j.1469-8749.1992.tb11406.x Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1005 Titles: – TitleFull: 18q- chromosomal abnormality in a phenotypically normal 2 1/2-year-old male with autism. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Seshadri K – PersonEntity: Name: NameFull: Wallerstein R – PersonEntity: Name: NameFull: Burack G IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 11 Text: 1992 Nov Type: published Y: 1992 Identifiers: – Type: issn-print Value: 0012-1622 Numbering: – Type: volume Value: 34 – Type: issue Value: 11 Titles: – TitleFull: Developmental medicine and child neurology Type: main |
| ResultId | 1 |