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Deletion of Chromosome 2 q37 and Autism: A Distinct Subtype?

dc.contributor.authorBurmeister, Margit L.en_US
dc.contributor.authorGhaziuddin, Mohammaden_US
dc.date.accessioned2006-09-11T15:03:18Z
dc.date.available2006-09-11T15:03:18Z
dc.date.issued1999-06en_US
dc.identifier.citationGhaziuddin, 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.issn0162-3257en_US
dc.identifier.issn1573-3432en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44617
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=10425588&dopt=citationen_US
dc.description.abstractSeveral 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.extent1335941 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Mediaen_US
dc.subject.otherNeuropsychologyen_US
dc.subject.otherClinical Psychologyen_US
dc.subject.otherPsychologyen_US
dc.subject.otherPediatricsen_US
dc.subject.otherDevelopmental Psychologyen_US
dc.subject.otherAutismen_US
dc.subject.otherChromosome 2en_US
dc.subject.otherGeneticsen_US
dc.titleDeletion of Chromosome 2 q37 and Autism: A Distinct Subtype?en_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelSocial Worken_US
dc.subject.hlbsecondlevelPsychologyen_US
dc.subject.hlbsecondlevelPsychiatryen_US
dc.subject.hlbsecondlevelPediatricsen_US
dc.subject.hlbtoplevelSocial Sciencesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Psychiatry, Division of Child Psychiatry, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Psychiatry and Human Genetics, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid10425588en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44617/1/10803_2004_Article_422215.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1023/A:1023088207468en_US
dc.identifier.sourceJournal of Autism and Developmental Disordersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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