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OTX2 mutations contribute to the otocephaly-dysgnathia complex
  1. Correspondence to Dr Nicolas Chassaing, Service de Génétique Médicale, Pavillon Lefebvre, CHU Purpan, Place du Dr Baylac, Toulouse 31059, Cedex 9, France; chassaing.n{at}chu-toulouse.fr
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Citation

Chassaing N, Sorrentino S, Davis EE, et al
OTX2 mutations contribute to the otocephaly-dysgnathia complex

Publication history

  • Received March 14, 2012
  • Accepted April 11, 2012
  • First published May 10, 2012.
Online issue publication 
April 27, 2016

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