References in periodicals archive ?
Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletion.
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy.
Diagnostic criteria for facioscapulohumeral muscular dystrophy.
Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy.
Facioscapulohumeral muscular dystrophy presenting isolated monomelic lower limb atrophy.