Carrier detection in Duchenne muscular dystrophy using molecular methods. [electronic resource]
Producer: 20140121Description: 1102-10 p. digitalISSN:- 0971-5916
- Alleles
- Blotting, Southern
- Chromosomes, Human, X
- Dystrophin -- genetics
- Female
- Gene Deletion
- Gene Duplication
- Genetic Linkage
- Genetic Markers
- Heterozygote
- Humans
- Male
- Microsatellite Repeats
- Muscular Dystrophy, Duchenne -- diagnosis
- Mutation
- Point Mutation
- Polymerase Chain Reaction
- Reproducibility of Results
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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