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- W2005045844 abstract "The tendency for red blood cells to assume a sickled shape under conditions of low oxygenation has been demonstrated predominantly in the Negro race.1Patients exhibiting this phenomenon have been classified as having sickle-cell trait, an asymptomatic carrier state, or sickle-cell anemia, a hemolytic disease with occlusive vascular complications and shortened life span. Renewed clinical interest in these entities has followed recent developments in the study of human hemoglobins. In 1949, Pauling, Itano, Singer, and Wells2proved by means of electrophoresis that the hemoglobin in patients with sicklecell anemia (sickle-cell hemoglobin, or hemoglobin S) differs from normal adult hemoglobin (hemoglobin A). Furthermore, familial electrophoretic studies2and the genetic investigations of Neel3established the hereditary basis for the sickling phenomenon. The inheritance of the gene for sicklecell hemoglobin from one parent and the gene for hemoglobin A from another parent, constitutes the sickle-cell trait and represents a" @default.
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- W2005045844 date "1957-11-01" @default.
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- W2005045844 title "Ocular Manifestations of Sickle-Cell Disease" @default.
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- W2005045844 doi "https://doi.org/10.1001/archopht.1957.00940010673005" @default.
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