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"Case BIII.1 had mild microcytic anaemia, reticulocytosis, and increased ferritin levels; 17% of stomatocytes were detected at blood smear examination (XREF_TABLE and XREF_FIG); the molecular testing for HBB gene revealed the presence of the splicing mutation c.93-21G> A at heterozygote level, confirming the beta-thalassemia trait."