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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Hlavní autoři: Clemens, P R, Fenwick, R G, Chamberlain, J S, Gibbs, R A, de Andrade, M, Chakraborty, R, Caskey, C T
Médium: Artigo
Jazyk:Inglês
Vydáno: 1991
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683265/
https://ncbi.nlm.nih.gov/pubmed/1928100
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