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19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation
  1. Correspondence to Dr V Malan, Service de Cytogénétique et d’Embryologie, Hôpital Necker-Enfants Malades, 149, rue de Sèvres, 75743 Paris Cedex 15, France; Valerie.malan{at}nck.aphp.fr
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Citation

Malan V, Raoul O, Firth HV, et al
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation

Publication history

  • Received August 28, 2008
  • Revised November 21, 2008
  • Accepted December 1, 2008
  • First published January 6, 2009.
Online issue publication 
September 01, 2009

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