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Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani–Lenz-like non-syndromic oligosyndactyly
- Correspondence to Professor Dr Philippe Debeer, Centre of Human Genetics, University Hospitals Leuven, Herestraat 49, Leuven 3000, Belgium; philippe.debeer{at}uzleuven.be
Citation
Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani–Lenz-like non-syndromic oligosyndactyly
Publication history
- Received October 20, 2009
- Revised January 25, 2010
- Accepted February 13, 2010
- First published July 7, 2010.
Online issue publication
April 27, 2016
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© 2010, 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.