Persistent URL of this record https://hdl.handle.net/1887/97286
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Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity
- All authors
- Sacconi, S.; Camano, P.; Greef, J.C. de; Lemmers, R.J.L.F.; Salviati, L.; Boileau, P.; Arregui, A.L.D.; Maarel, S.M. van der; Desnuelle, C.
- Date
- 2012-01-31
- Journal
- Journal of Medical Genetics
- Volume
- 49
- Issue
- 1
- Pages
- 41 - 46