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Unusual combination of genetic defects in a Sicilian boy: Gγ Aγ δβ thalassemia, Gγ Aγ heterocellular HPFH, βº thalassemia, and albinism

✍ Scribed by Schilirò, G. ;Pavone, L. ;Romeo, M. A. ;Russo, A. ;Musumeci, S. ;Russo, G. ;Opitz, John M.

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