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- W1580436909 abstract "Summary This report describes the clinical and haematological findings in three siblings homozygous for Gγ δβ thalassaemia in an Indian family. There was a mild to moderate anaemia and markedly abnormal red cell morphology. Haemoglobin analysis showed 100% Hb F, solely of the Gγ type, with a pancellular but uneven distribution. Considerable chain imbalance was detectable in globin synthesis studies. In contrast to the five previously reported cases, these children were essentially asymptomatic and have never required transfusions." @default.
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- W1580436909 date "1981-06-01" @default.
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- W1580436909 title "Homozygous<sup>G</sup>γλβ thalassaemia" @default.
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- W1580436909 doi "https://doi.org/10.1111/j.1365-2257.1981.tb01321.x" @default.
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