A carregar...

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,...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Clemens, P R, Fenwick, R G, Chamberlain, J S, Gibbs, R A, de Andrade, M, Chakraborty, R, Caskey, C T
Formato: Artigo
Idioma:Inglês
Publicado em: 1991
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683265/
https://ncbi.nlm.nih.gov/pubmed/1928100
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!