Search..

Validating credentials, please wait...
Author information:

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.

Leave a Reply

Your email address will not be published. Required fields are marked *

Translate »