Article info
PDFCopy-number variation
Original article
Identification of the first recurrent PAR1 deletion in Léri-Weill dyschondrosteosis and idiopathic short stature reveals the presence of a novel SHOX enhancer
- Correspondence to Dr Karen Elise Heath, Instituto de Genética Médica y Molecular (INGEMM), Hospital Universitario La Paz, P° Castellana 261, 28046 Madrid, Spain; kheath.hulp{at}salud.madrid.org
Citation
Identification of the first recurrent PAR1 deletion in Léri-Weill dyschondrosteosis and idiopathic short stature reveals the presence of a novel SHOX enhancer
Publication history
- Received December 7, 2011
- Revised May 30, 2012
- Accepted May 31, 2012
- First published July 11, 2012.
Online issue publication
April 27, 2016
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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.