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Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders
- Correspondence to: A Philippe INSERM U781, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France;kinabalu{at}free.fr
Citation
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders
Publication history
- Received April 6, 2006
- Accepted June 21, 2006
- Revised June 20, 2006
- First published July 13, 2006.
Online issue publication
April 27, 2016
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Copyright 2006 Journal of Medical Genetics