Deletion of Chromosome 2 q37 and Autism: A Distinct Subtype?
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| Title: | Deletion of Chromosome 2 q37 and Autism: A Distinct Subtype? |
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| Authors: | Ghaziuddin M (AUTHOR), Burmeister M (AUTHOR) |
| Source: | Journal of Autism & Developmental Disorders. Jun1999, Vol. 29 Issue 3, p259-263. 5p. |
| Abstract: | Several reports have described the occurrence of chromosome abnormalities in autism, a neuro-developmental disorder characterized by social deficits, communication impairment, and a restricted range of interests. These include the fragile X abnormality and 15q duplications. In this report, we describe two cases of chromosome 2q37 and review the literature on this topic. We propose that deletion of the distal portion of the long arm of chromosome 2 (2q37) may be associated with some cases of autism and with a distinct phenotype. Increased awareness of the dysmorphic features associated with 2q37 deletions may aid in the molecular genetic analysis of this chromosome anomaly and clarify its relationship with autism. [ABSTRACT FROM AUTHOR] |
| Copyright of Journal of Autism & Developmental Disorders is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Psychology and Behavioral Sciences Collection |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: pbh DbLabel: Psychology and Behavioral Sciences Collection An: 106080012 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Deletion of Chromosome 2 q37 and Autism: A Distinct Subtype? – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Ghaziuddin+M%22">Ghaziuddin M</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Burmeister+M%22">Burmeister M</searchLink> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Journal+of+Autism+%26+Developmental+Disorders%22">Journal of Autism & Developmental Disorders</searchLink>. Jun1999, Vol. 29 Issue 3, p259-263. 5p. – Name: Abstract Label: Abstract Group: Ab Data: Several reports have described the occurrence of chromosome abnormalities in autism, a neuro-developmental disorder characterized by social deficits, communication impairment, and a restricted range of interests. These include the fragile X abnormality and 15q duplications. In this report, we describe two cases of chromosome 2q37 and review the literature on this topic. We propose that deletion of the distal portion of the long arm of chromosome 2 (2q37) may be associated with some cases of autism and with a distinct phenotype. Increased awareness of the dysmorphic features associated with 2q37 deletions may aid in the molecular genetic analysis of this chromosome anomaly and clarify its relationship with autism. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Journal of Autism & Developmental Disorders is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=pbh&AN=106080012 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1023/a:1023088207468 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 259 Titles: – TitleFull: Deletion of Chromosome 2 q37 and Autism: A Distinct Subtype? Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ghaziuddin M – PersonEntity: Name: NameFull: Burmeister M IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: Jun1999 Type: published Y: 1999 Identifiers: – Type: issn-print Value: 01623257 Numbering: – Type: volume Value: 29 – Type: issue Value: 3 Titles: – TitleFull: Journal of Autism & Developmental Disorders Type: main |
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