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- W2000538831 abstract "We have used restriction endonucleases for mapping the δ globin gene within the genomic DNA obtained from an individual homozygous for δ thalassemia. The results of our analyses indicate that δ thalassemia is not due to a detectable structural gene deletion as found in α thalassemia, δβ thalassemia or hereditary persistance of fetal hemoglobin, but probably consist of molecular lesions similar to those found in the β° or β+ thalassemias." @default.
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- W2000538831 date "1981-04-01" @default.
- W2000538831 modified "2023-09-24" @default.
- W2000538831 title "A case of homozygous δ thalassemia not due to a deletion of the δ globin structural gene" @default.
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- W2000538831 doi "https://doi.org/10.1016/0006-291x(81)90722-1" @default.
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