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CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype
  1. Correspondence to Dr C M A van Ravenswaaij-Arts, Department of Genetics, University Medical Centre Groningen, PO Box 30.001, 9700 RB Groningen, The Netherlands; c.m.a.van.ravenswaaij{at}medgen.umcg.nl
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Bergman JEH, Janssen N, Hoefsloot LH, et al
CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype

Publication history

  • Received November 29, 2010
  • Revised February 3, 2011
  • Accepted February 8, 2011
  • First published March 4, 2011.
Online issue publication 
April 27, 2011

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