Fig. 1From: Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disordersDescription of the nine pedigrees with FPD/AML. : Healthy relatives. : Mutated patient without thrombocytopenia. : Mutated patient with thrombocytopenia. : Patient diagnosed with malignancy. In each family a black arrow designs the probandBack to article page