DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.

Thirteen marker loci localised on the short arm of the X chromosome are available for use in genetic studies for Duchenne muscular dystrophy (DMD). This large number of probes detecting about 20 RFLPs encouraged us to set up a standard procedure using a sequence of selected probes and restriction en...

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Detalhes bibliográficos
Main Authors: Bakker, E, Bonten, E J, De Lange, L F, Veenema, H, Majoor-Krakauer, D, Hofker, M H, Van Ommen, G J, Pearson, P L
Formato: Artigo
Idioma:Inglês
Publicado em: 1986
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049839/
https://ncbi.nlm.nih.gov/pubmed/2879929
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