Validation of Optical Genome Mapping for the Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy
Author:
Publisher
Elsevier BV
Subject
Molecular Medicine,Pathology and Forensic Medicine
Reference20 articles.
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2. Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD;de Greef;Hum Mutat,2009
3. A unifying genetic model for facioscapulohumeral muscular dystrophy;Lemmers;Science,2010
4. Facioscapulohumeral muscular dystrophy: consequences of chromatin relaxation;van der Maarel;Curr Opin Neurol,2012
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