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Numerous deletional thalassemias have been reported so far, involving one or several globin genes in combination.[1][1] A deletion specifically targeted on the fetal β-like genes was first described in 1983 and was characterized as a deletion-fusion removing the 3γ end of Gγ-gene and the 5γ end

First case of -thalassemia in association with a S allele: a pitfall in the neonatal screening for sickle cell disease