Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms.

To improve carrier detection and prenatal diagnosis for Duchenne and Becker muscular dystrophy families, we determined allele frequencies and measures of variation for four (dC-dA)n.(dG-dT)n loci identified within a deletion-prone region of the human dystrophin gene. The loci are highly polymorphic,...

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Bibliografiska uppgifter
Huvudupphovsmän: Clemens, P R, Fenwick, R G, Chamberlain, J S, Gibbs, R A, de Andrade, M, Chakraborty, R, Caskey, C T
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1991
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683265/
https://ncbi.nlm.nih.gov/pubmed/1928100
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