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Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia

The amount of fetal hemoglobin (Hb F) in erythrocytes of patients with sickle cell anemia (Hb SS disease) was measured by two methods: (a) photometry of individual cells stained for Hb F by the Kleihauer-Betke technique; and (b) chemical assay of alkali-resistant hemoglobin in cells distributed acco...

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Autores principales: Bertles, John F., Milner, Paul F. A.
Formato: Artigo
Lenguaje:Inglês
Publicado: 1968
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC297333/
https://ncbi.nlm.nih.gov/pubmed/5666109
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