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Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
  1. Dr J R Vermeesch, Center for Human Genetics, Herestraat 49, 3000 Leuven, Belgium; joris.vermeesch{at}uz.kuleuven.ac.be
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Citation

Hannes FD, Sharp AJ, Mefford HC, et al
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant

Publication history

  • Received October 5, 2007
  • Revised December 28, 2007
  • Accepted January 7, 2008
  • First published June 11, 2008.
Online issue publication 
April 08, 2009

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