1. Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity. Issue 1 (7th October 2011) Authors: Sacconi, Sabrina; Camaño, Pilar; de Greef, Jessica C; Lemmers, Richard J L F; Salviati, Leonardo; Boileau, Pascal; Lopez de Munain Arregui, Adolfo; van der Maarel, Silvère M; Desnuelle, Claude Journal: Journal of medical genetics Issue: Volume 49:Issue 1(2012) Page Start: 41 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗