Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2008.02314.x/fullpdf
Reference30 articles.
1. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy;Wijmenga;Nature Genetics,1992
2. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit;Van Deutekom;Human Molecular Genetics,1993
3. Facioscapulohumeral muscular dystrophy (review);Fitzsimons;Current Opinion in Neurology,1999
4. Facioscapulohumeral muscular dystrophy;Tawil;Muscle and Nerve,2006
5. Facioscapulohumeral muscular dystrophy in early childhood;Brouwer;Archives of Neurolology,1994
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