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Restriction mapping of a new deletion responsible for (G)γ(δβ)(o) thalassaemia
DNA from individuals heterozygous for (G)γ(δβ)(o) thalassaemia has been studied by restriction endonuclease analysis. The results reveal a new molecular defect associated with this condition. A total of three defects is now responsible for the one single phenotype, thereby emphasising the complex re...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
1981
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC327644/ https://ncbi.nlm.nih.gov/pubmed/6278449 |
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