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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
  1. Correspondence to:
 Dr N P Carter
 The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK; npcsanger.ac.uk
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Citation

Shaw-Smith C, Redon R, Rickman L, et al
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 01, 2004

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