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Original article
Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling
- Correspondence to Professor Rossella Tupler, Department of Biomedical Sciences, University of Modena and Reggio Emilia, Via Campi 287, Modena 41125, Italy; rossella.tupler{at}unimore.it
Citation
Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling
Publication history
- Received August 25, 2011
- Revised December 1, 2011
- Accepted December 6, 2011
- First published January 3, 2012.
Online issue publication
April 27, 2016
Article Versions
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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.