Direct identification of sickle cell anemia by blot hybridization.
Several reports have been published on the use of polymorphisms found in the human hemoglobin genes as a means for prenatal diagnosis of sickle cell anemia. The disadvantages of this approach reside in its limited application and the need for family analysis. Here we report that, by use of restricti...
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| Yayımlandı: | Proc Natl Acad Sci U S A |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
National Academy of Sciences
1981
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC320336/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6272289/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.78.8.5081 |
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