Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome.
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Summary
The linkage data obtained suggest that both the DMD and BMD loci are located in the same region (p21) on the short arm of the X chromosome at a distance of about 15 to 20 cM from the 754 locus.
- Type
- article
- Published
- 1985-06-01
- Cited by
- 11
- References
- 10
- Access
- Open access
- OpenAlex
- https://openalex.org/W2011632633
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:43075154
Keywords
Genetics, Restriction fragment length polymorphism, Genetic linkage, Locus (genetics), Biology
References
- Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.
- Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.
- The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy.
- Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.
- Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysis
- Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes.
- Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome.
- Pathogenesis of Human Muscular Dystrophies
Cited by
- Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers
- Modelling FKRP and fukutin deficiency in zebrafish
- Molecular genetics of Duchenne and Becker muscular dystrophy.
- Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy
- Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms
- Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.
- Becker muscular dystrophy recombinant DNA studies in identical twins
- Diagnosis of genetic disease using recombinant DNA
- Molecular analysis of human muscular dystrophies
- Sporadic cases in Duchenne muscular dystrophy
- DNA Polymorphisms and Fetal Sexing for X-Linked Disorders with Chorionic Biopsy
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