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Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders
  1. Correspondence to:
 A Philippe
 INSERM U781, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France;kinabalu{at}free.fr
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Citation

Jacquemont M, Sanlaville D, Redon R, et al
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 
November 03, 2006

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