Article info
PDFDevelopmental defects
Original article
OTX2 mutations contribute to the otocephaly-dysgnathia complex
- 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
Citation
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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© 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.