FSHD-like patients without 4q35 deletion
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference24 articles.
1. Location of facioscapulohumeral muscular dystrophy gene on chromosome 4;Wijmenga;Lancet,1990
2. Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization;Wijmenga;Genomics,1991
3. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy;Wijmenga;Nat. Genet.,1992
4. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit;van Deutekom;Hum. Mol. Genet.,1993
5. Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy;Hewitt;Hum. Mol. Genet.,1994
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