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• W2128346477 abstract "DNA has been prepared from peripheral blood or cultured skin fibroblasts obtained from three Sicilian and one Greek δβ-thalassemia homozygotes. Globin-gene analysis was carried out using a cDNAβ probe, and the results indicate that δβ-thalassemia has arisen from a deletion of the β-globin genes. A similar result was obtained using DNA prepared from cultured skin fibroblasts from an individual homozygous for the Negro form of hereditary persistence of fetal hemoglobin (HPFH). In both cases, the deletion has spared the Gγ and Aγ loci directing the γ chains of hemoglobin F, but it has not been possible to demonstrate any difference between the size of the deletion involved in the production of δβ-thalassemia and that which gave rise to HPFH. These experiments provide further direct evidence that deletions of critical areas of the γ-δ-β gene cluster result in persistent γ chain synthesis in adult life." @default.
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• W2128346477 date "1976-09-01" @default.
• W2128346477 modified "2023-10-15" @default.
• W2128346477 title "δβ-Thalassemia is due to a gene deletion" @default.
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• W2128346477 doi "https://doi.org/10.1016/0092-8674(76)90053-2" @default.
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