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Original article
Identification of a novel DLX5 mutation in a family with autosomal recessive split hand and foot malformation
- Correspondence to Dr Fowzan S Alkuraya, Developmental Genetics Unit, King Faisal Specialist Hospital and Research Center, MBC-03 PO BOX 3354, Riyad 11211, Saudi Arabia; falkuraya{at}kfshrc.edu.sa
Citation
Identification of a novel DLX5 mutation in a family with autosomal recessive split hand and foot malformation
Publication history
- Received October 6, 2011
- Revised November 2, 2011
- Accepted November 3, 2011
- First published November 25, 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.