The X chromosome in Duchenne's muscular dystrophy
- 1 March 1976
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 9 (3), 371-373
- https://doi.org/10.1111/j.1399-0004.1976.tb01589.x
Abstract
A search for deficiencies on 1 human X chromosome of 4 obligatory and 4 probable heterozygotes for Duchenne''s muscular dystrophy was unsuccessful. This probably excludes deficiencies larger than half the width of any band or interband.Keywords
This publication has 9 references indexed in Scilit:
- Muscular dystrophy in Northern IrelandAnnals of Human Genetics, 2007
- Genetic-epidemiological studies in progressive muscular dystrophy.Journal of Medical Genetics, 1971
- Mutation rate in Duchenne type of muscular dystrophy.Journal of Medical Genetics, 1970
- Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy.Journal of Medical Genetics, 1966
- Duchenne's Muscular Dystrophy and the Xg Blood Groups: a Search for LinkageJournal of Medical Genetics, 1965
- PROGRESSIVE MUSCULAR DYSTROPHY OF THE DUCHENNE TYPE IN FEMALES AND ITS MODE OF INHERITANCEBrain, 1960
- MUSCULAR DYSTROPHY IN CHILDHOOD. THE GENETIC ASPECT.Annals of Human Genetics, 1958
- MUSCULAR DYSTROPHY IN NORTHERN IRELANDAnnals of Human Genetics, 1958
- MUSCULAR DYSTROPHY IN NORTHERN IRELAND.Annals of Human Genetics, 1955