Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference20 articles.
1. Genetic counselling in facioscapulohumeral muscular dystrophy;Lunt;J Med Genet,1991
2. Facioscapulohumeral muscular dystrophy (FSHD): design of natural history study and results of baseline testing, FSH-DY group;Tawil;Neurology,1994
3. Phenotypic–genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy;Lunt;Muscle Nerve,1995
4. Facioscapulohumeral muscular dystrophy in the Dutch population;Padberg;Muscle Nerve,1995
5. The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD);Upadhyaya;Am J Hum Genet,1992
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