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CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype
- 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
Citation
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, 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.