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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| 發表在: | Nucleic Acids Res |
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| Principais autores: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Oxford University Press
1988
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| 在線閱讀: | 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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