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Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene
  1. Correspondence to:
 Lionel Van Maldergem
 10 rue de la Treille, B-1050 Brussels, Belgium; vmald{at}skypro.be
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Citation

Van Maldergem L, Siitonen HA, Jalkh N, et al
Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene

Publication history

  • Accepted May 11, 2005
  • Revised May 9, 2005
  • First published June 17, 2005.
Online issue publication 
April 27, 2016

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