Format

Send to

Choose Destination
Am J Hum Genet. 2006 Sep;79(3):500-13. Epub 2006 Jul 25.

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation.

Author information

1
Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada. frid@interchange.ubc.ca

Erratum in

  • Am J Hum Genet. 2006 Dec;79(6):1135. Armstrong, Linlea [added].

Abstract

The cause of mental retardation in one-third to one-half of all affected individuals is unknown. Microscopically detectable chromosomal abnormalities are the most frequently recognized cause, but gain or loss of chromosomal segments that are too small to be seen by conventional cytogenetic analysis has been found to be another important cause. Array-based methods offer a practical means of performing a high-resolution survey of the entire genome for submicroscopic copy-number variants. We studied 100 children with idiopathic mental retardation and normal results of standard chromosomal analysis, by use of whole-genome sampling analysis with Affymetrix GeneChip Human Mapping 100K arrays. We found de novo deletions as small as 178 kb in eight cases, de novo duplications as small as 1.1 Mb in two cases, and unsuspected mosaic trisomy 9 in another case. This technology can detect at least twice as many potentially pathogenic de novo copy-number variants as conventional cytogenetic analysis can in people with mental retardation.

PMID:
16909388
PMCID:
PMC1559542
DOI:
10.1086/507471
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Elsevier Science Icon for PubMed Central
Loading ...
Support Center