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,...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Clemens, P R, Fenwick, R G, Chamberlain, J S, Gibbs, R A, de Andrade, M, Chakraborty, R, Caskey, C T
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1991
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683265/
https://ncbi.nlm.nih.gov/pubmed/1928100
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia