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- W2407314229 abstract "Abstract The clinical, hematologic, and genetic manifestations of the Hgb E syndromes are described. Hgb E trait, the heterozygous form of Hgb E, is unaccompanied by any disability. Thalassemia-Hgb E disease simulates thalassemia major in almost every respect and results from the mating of a carrier of the gene for thalassemia with an individual who harbors the gene for Hgb E. Homozygous Hgb E disease is manifest as a mild microcytic, normochromic anemia, characterized by large numbers of target cells. Theoretical considerations relative to the genetic background of thalassemia-Hgb E disease and the thalassemia syndromes are discussed." @default.
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- W2407314229 date "1956-03-01" @default.
- W2407314229 modified "2023-09-23" @default.
- W2407314229 title "Studies on hemoglobin E. I. The clinical, hematologic, and genetic characteristics of the hemoglobin E syndromes." @default.
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