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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.

Type

Journal article

Journal

Lancet

Publication Date

1981

Volume

1

Pages

527 - 529

Keywords

Adolescent Adult Case Report Child Chromosome Deletion Cyprus Female Globins/*genetics Homozygote Human Male Pedigree Phenotype Support, Non-U.S. Gov't Thalassemia/*genetics