Diagnosis and molecular characterization of a novel α0‐thalassemia deletion (–Kozani) found in a Greek child with unexplained microcytic hypochromic anemia. (12th June 2017) - Makis, A.; Georgiou, I.; Traeger‐Synodinos, J.; Chaliasos, N.; Grosso, M.; Gambale, A.; Iolascon, A.