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Duplications of the critical Rubinstein–Taybi deletion region on chromosome 16p13.3 cause a novel recognisable syndrome
- Correspondence to Professor Dr Koen Devriendt, Center for Human Genetics, K.U. Leuven, Herestraat 49 box 602, Leuven 3000, Belgium; koenraad.devriendt{at}uzleuven.be
Citation
Duplications of the critical Rubinstein–Taybi deletion region on chromosome 16p13.3 cause a novel recognisable syndrome
Publication history
- Received June 24, 2009
- Accepted July 19, 2009
- First published October 14, 2009.
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.