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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Bibliografiske detaljer

Udgivet i:	Proc Natl Acad Sci U S A
Principais autores:	Geever, R F, Wilson, L B, Nallaseth, F S, Milner, P F, Bittner, M, Wilson, J T
Format:	Artigo
Sprog:	Inglês
Udgivet:	National Academy of Sciences 1981
Fag:	Research Article
Online adgang:	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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