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Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia
- Correspondence to Dr rer. nat. Eva Klopocki, Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany; eva.klopocki{at}charite.de
Citation
Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia
Publication history
- Received March 9, 2012
- Revised May 17, 2012
- Accepted May 29, 2012
- First published June 20, 2012.
Online issue publication
July 11, 2012
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© 2012, 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.