Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization
- 30 April 1991
- Vol. 9 (4) , 570-575
- https://doi.org/10.1016/0888-7543(91)90348-i
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Location of facioscapulohumeral muscular dystrophy gene on chromosome 4The Lancet, 1990
- Facioscapulohumeral muscular dystrophy gene in Dutch families is not linked to markers for familial adenomatous polyposis on the long arm of chromosome 5Journal of the Neurological Sciences, 1990
- Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias.Journal of Medical Genetics, 1989
- Recombination events suggest potential sites for the Huntington's disease geneNeuron, 1989
- Isolation and mapping of a polymorphic DNA sequence pH30 on chromosome 4 [HGM provisional no. IMS 139]Nucleic Acids Research, 1989
- RETINAL VASCULAR ABNORMALITIES IN FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHYBrain, 1987
- Hearing loss in facioscapulohumeral dystrophyEuropean Journal of Pediatrics, 1986
- An algorithm to improve the computational efficiency of genetic linkage analysisComputers and Biomedical Research, 1985
- Linkage analysis and family classification under heterogeneityAnnals of Human Genetics, 1983