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Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
Published on: February 21, 2015
Brief report: A case of autism with interstitial deletion of chromosome 13
M M Steele1, M Al-Adeimi, V M Siu
1Department of Psychiatry, University of Western Ontario, London Health Sciences Centre, Canada. margaret.steele@lhsc.on.ca
Journal of Autism and Developmental Disorders
|July 14, 2001
Abstract:
A case of an 18-year-old male who meets the DSM-IV criteria for autistic disorder and borderline intelligence is described. Cytogenetic evaluation revealed a karyotype of 46, XY, del(13)(q14q22). The relevance of this case to the etiology of autism is discussed.
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