Daniela Leone

The β-Thalassemias

Identification and characterization of a spinal muscular atrophy-determining gene

Insertions, substitutions, and the origin of microsatellites

Microsatellites: simple sequences with complex evolution

Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations

Beta‐thalassaemia intermedia: is it possible consistently to predict phenotype from genotype?

The C–T substitution in the distal CACCC box of the β‐globin gene promoter is a common cause of silent β thalassaemia in the Italian population

A spontaneous mutation produced a novel elongated beta-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotype [letter]