Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification.

The application of recombinant DNA technology to prenatal diagnosis of many recessively inherited X-linked diseases is complicated by a high frequency of heterogeneous, new mutations (1). Partial gene deletions account for more than 50% of Duchenne muscular dystrophy (DMD) lesions, and approximately...

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Detalles Bibliográficos

Publicado en:	Nucleic Acids Res
Autores principales:	Chamberlain, J S, Gibbs, R A, Ranier, J E, Nguyen, P N, Caskey, C T
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	Oxford University Press 1988
Acceso en línea:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC339001/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3205741/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/16.23.11141
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