DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
van der Maarel SM, Deidda G, Lemmers RJ. , et al.
De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10.
Am J Hum Genet 2000;
66 (01) 26-35
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