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Original article
2q31.1 microdeletion syndrome: redefining the associated clinical phenotype

Authors

  1. Correspondence to Dr Philippe Debeer, Centre for Human Genetics, University Hospitals Leuven, Herestraat 49, 3000 Leuven, Belgium; philippe.debeer{at}uzleuven.be
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Citation

Dimitrov B, Balikova I, de Ravel T, et al
2q31.1 microdeletion syndrome: redefining the associated clinical phenotype
Journal of Medical Genetics 2011;48:98-104.

Publication history

  • Received March 31, 2010
  • Revised September 22, 2010
  • Accepted September 30, 2010
  • First published November 10, 2010.
Online issue publication 
April 27, 2016

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© 2011, 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.