Prenatal diagnosis of beta thalassaemia based on restriction endonuclease analysis of amplified fetal DNA.
In the Mediterranean area, 50% of the beta thalassaemia mutations abolish or create a restriction endonuclease site in the beta globin gene. This study describes a new procedure for prenatal detection of these beta thalassaemia defects based on the direct visualisation, on an ethidium bromide staine...
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| Publicado no: | J Med Genet |
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| Principais autores: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
1989
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015619/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2738898/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.26.6.363 |
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