4q35 molecular probes for the diagnosis and genetic counseling of facioscapulohumeral muscular dystrophy
- 1 July 1994
- journal article
- letter
- Published by Wiley in Annals of Neurology
- Vol. 36 (1) , 117-118
- https://doi.org/10.1002/ana.410360128
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination eventsNature Genetics, 1993
- Transmission of de-novo mutation associated with facioscapulohumeral muscular dystrophyThe Lancet, 1992
- Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophyNature Genetics, 1992