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Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features
- Correspondence to: Dr N P Carter The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK; npcsanger.ac.uk
Citation
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features
Publication history
- Accepted January 18, 2004
- Revised January 8, 2004
- First published April 1, 2004.
Online issue publication
April 27, 2016
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Copyright 2004 Journal of Medical Genetics