Deletion of Chromosome 2 q37 and Autism: A Distinct Subtype?
dc.contributor.author | Burmeister, Margit L. | en_US |
dc.contributor.author | Ghaziuddin, Mohammad | en_US |
dc.date.accessioned | 2006-09-11T15:03:18Z | |
dc.date.available | 2006-09-11T15:03:18Z | |
dc.date.issued | 1999-06 | en_US |
dc.identifier.citation | Ghaziuddin, Mohammad; Burmeister, Margit; (1999). "Deletion of Chromosome 2 q37 and Autism: A Distinct Subtype?." Journal of Autism and Developmental Disorders 29(3): 259-263. <http://hdl.handle.net/2027.42/44617> | en_US |
dc.identifier.issn | 0162-3257 | en_US |
dc.identifier.issn | 1573-3432 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/44617 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=10425588&dopt=citation | en_US |
dc.description.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. | en_US |
dc.format.extent | 1335941 bytes | |
dc.format.extent | 3115 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Kluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Media | en_US |
dc.subject.other | Neuropsychology | en_US |
dc.subject.other | Clinical Psychology | en_US |
dc.subject.other | Psychology | en_US |
dc.subject.other | Pediatrics | en_US |
dc.subject.other | Developmental Psychology | en_US |
dc.subject.other | Autism | en_US |
dc.subject.other | Chromosome 2 | en_US |
dc.subject.other | Genetics | en_US |
dc.title | Deletion of Chromosome 2 q37 and Autism: A Distinct Subtype? | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Public Health | en_US |
dc.subject.hlbsecondlevel | Social Work | en_US |
dc.subject.hlbsecondlevel | Psychology | en_US |
dc.subject.hlbsecondlevel | Psychiatry | en_US |
dc.subject.hlbsecondlevel | Pediatrics | en_US |
dc.subject.hlbtoplevel | Social Sciences | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Psychiatry, Division of Child Psychiatry, University of Michigan, Ann Arbor, Michigan | en_US |
dc.contributor.affiliationum | Department of Psychiatry and Human Genetics, University of Michigan, Ann Arbor, Michigan | en_US |
dc.contributor.affiliationumcampus | Ann Arbor | en_US |
dc.identifier.pmid | 10425588 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/44617/1/10803_2004_Article_422215.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1023/A:1023088207468 | en_US |
dc.identifier.source | Journal of Autism and Developmental Disorders | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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