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- W2013984857 abstract "Summary. Six individuals in four Indian families have 25–30% foetal haemoglobin in which the two types of γ chains (the Gγ chain with glycine in position 136 and the Aγ chain with alanine in that position) are present in a ratio of 70:30. It is suggested that these heterozygotes form a distinct subgroup of the HbGγ HbAγ class of the hereditary persistence of foetal haemoglobin. In three relatives this HPFH condition occurs together with β-thalassaemia. It is concluded that the β-thalassaemia is of the type in which the ratio of Gγ:Aγ chains is 3:1 as in the newborn." @default.
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- W2013984857 date "1973-07-01" @default.
- W2013984857 modified "2023-09-26" @default.
- W2013984857 title "A Second Type of Hereditary Persistence of Foetal Haemoglobin in India" @default.
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- W2013984857 doi "https://doi.org/10.1111/j.1365-2141.1973.tb01722.x" @default.
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