Diagnostic criteria for facioscapulohumeral muscular dystrophy
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference8 articles.
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2. DNA marker applicable to presymptomatic and prenatal diagnosis of Facioscapulohumeral disease;Upadhyaya;Lancet,1990
3. Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization;Wijmenga;Genomics,1991
4. Naissance et métamorphoses de la myopathie atrophique progressive de Landouzy et Dejerine;Sorrel-Dejerine;Revue Neurologique (Paris),1982
5. Facioscapulohumeral dystrophy and the scapulohumeral syndrome;Munsat,1986
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