Carrier detection and prenatal molecular diagnosis in a Duchenne muscular dystrophy family without any affected relative available. [electronic resource]
Producer: 20020114Description: 149-53 p. digitalISSN:- 0003-3995
- Adult
- Alleles
- Amniotic Fluid -- metabolism
- Densitometry
- Dystrophin -- genetics
- Exons
- Family Health
- Female
- Gene Deletion
- Genetic Linkage
- Genetic Markers
- Heterozygote
- Homozygote
- Humans
- Male
- Muscular Dystrophy, Duchenne -- diagnosis
- Pedigree
- Polymerase Chain Reaction
- Polymorphism, Genetic
- Polymorphism, Restriction Fragment Length
- Pregnancy
- Prenatal Diagnosis
- Sex Determination Processes
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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