Detection of ΞΆ-globin chains in the cord
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Ausavarungnirun, Ruchanee; Winichagoon, Pranee; Fucharoen, Suthat; Epstein, Nava
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Article
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1998
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John Wiley and Sons
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English
β 42 KB
Fetuses with homozygous alpha-thalassemia 1, in which the deletion of all four alpha-globin genes results in the absence of any alpha-globin chains, are severely anemic with clinical features of hydrops fetalis. Definitive diagnosis of alpha-thalassemia 1 carriers is difficult since there are few re