A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q.
Open Access
- 1 October 1991
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 28 (10) , 665-671
- https://doi.org/10.1136/jmg.28.10.665
Abstract
Close linkage of a hypervariable DNA probe on chromosome 4q (pH30, locus D4S139) has been found with the locus for facioscapulohumeral disease. Three recombinants were identified in a total of 140 meioses, giving a maximum lod score of 36.77 at a recombination fraction of 0.02. All but two of the families studied proved informative with this probe; all informative families showed evidence of linkage (except one family with a single scorable meiosis), making genetic heterogeneity unlikely from our data. The close linkage and highly informative nature of the probe will make it suitable for clinical application in presymptomatic and prenatal diagnosis. We have also confirmed loose linkage with the marker (Mfd22, locus D4S171) used to establish the initial assignment of the disorder to chromosome 4.Keywords
This publication has 24 references indexed in Scilit:
- DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral diseaseThe Lancet, 1990
- Location of facioscapulohumeral muscular dystrophy gene on chromosome 4The Lancet, 1990
- Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.Journal of Medical Genetics, 1990
- A workshop on facioscapulohumeral (Landouzy-Dejerine) disease, Manchester, 16 to 17 November 1988.Journal of Medical Genetics, 1989
- A genetic linkage study of facioscapulohumeral (Landouzy-Dejerine) disease with 24 polymorphic DNA probes.Journal of Medical Genetics, 1989
- Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral disease.Journal of Medical Genetics, 1989
- Linkage analysis of French families with facioscapulohumeral muscular dystrophy.Journal of Medical Genetics, 1989
- An exclusion map for facioscapulohumeral (Landouzy-Dejerine) disease.Journal of Medical Genetics, 1989
- Factor XI gene (F11) is located on the distal end of the long arm of human chromosome 4Cytogenetic and Genome Research, 1989
- Linkage studies in facioscapulo-humeral muscular dystrophyMuscle & Nerve, 1988