Monozygotic twins with facioscapulohumeral dystrophy (FSHD): Implications for genotype/phenotype correlation
- 1 January 1995
- journal article
- research article
- Published by Wiley in Muscle & Nerve
- Vol. 18 (S13) , S50-S55
- https://doi.org/10.1002/mus.880181311
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Facioscapulohumeral muscular dystrophy (FSHD)Neurology, 1994
- Genetics of facioscapulohumeral muscular dystrophyNeurology, 1993
- Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination eventsNature Genetics, 1993
- Extreme variability of expression in monozygotic twins with FSH muscular dystrophyNeurology, 1993
- Chromosome 4q DNA rearrangement in monozygotic twins discordant for facioscapulohumeral muscular dystrophyHuman Mutation, 1993
- THE INFLUENCE OF HANDEDNESS ON THE DISTRIBUTION OF MUSCULAR WEAKNESS OF THE ARM IN FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHYBrain, 1992
- Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophyNature Genetics, 1992
- Uses and limitations of twin studiesZeitschrift für Neurologie, 1991
- Location of facioscapulohumeral muscular dystrophy gene on chromosome 4The Lancet, 1990
- Electrophoretic Separations of Large DNA Molecules by Periodic Inversion of the Electric FieldScience, 1986