PMID: 6111635Mar 7, 1981Paper

Molecular basis for mild forms of homozygous beta-thalassaemia

Lancet
D J WeatherallJ B Clegg

Abstract

Five Cypriots homozygous for beta +-thalassaemia have inherited deletion or non-deletion forms of alpha-thalassaemia that seem to have modified the usually severe clinical picture to that of mild thalassaemia intermedia. These observations have important implications for the antenatal diagnosis of beta-thalassaemia.

Citations

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