Linkage studies in facioscapulo-humeral muscular dystrophy
- 1 August 1988
- journal article
- research article
- Published by Wiley in Muscle & Nerve
- Vol. 11 (8), 833-835
- https://doi.org/10.1002/mus.880110806
Abstract
Possible linkage between the locus for autosomal dominant facioscapulohumeral muscular dystrophy and the locus for the constant region of the heavy chains of the IgG immunoglobulins (Gm) was tested in 1 kindred (23 affected and 18 unaffected sibs) using the polymorphic DNA probe D14S1, which is known to be closely linked with Gm. No linkage between the loci for the disease and the probe was found, and the lod scores suggested that the locus for facioscapulohumeral muscular dystrophy is not situated on the distal part of the long arm of chromosome 14.This publication has 3 references indexed in Scilit:
- Linkage studies in autosomal dominant facioscapulohumeral muscular dystrophyJournal of the Neurological Sciences, 1984
- Highly polymorphic DNA site D14S1 maps to the region of Burkitt lymphoma translocation and is closely linked to the heavy chain γ1 immunoglobulin locusProceedings of the National Academy of Sciences, 1982
- STUDIES IN DISORDERS OF MUSCLE. II. CLINICAL MANIFESTATIONS AND INHERITANCE OF FACIOSCAPULOHUMERAL DYSTROPHY IN A LARGE FAMILYAnnals of Internal Medicine, 1950