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GATA-1 Defects in Diamond-Blackfan Anemia: Phenotypic Characterization Points to a Specific Subset of DiseaseGenes, 2022, 13 (3), ⟨10.3390/genes13030447⟩
Article dans une revue
hal-03641414v1
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Next generation sequencing (NGS) interest in deciphering erythrocyte molecular defects' association in red cell disorders: Clinical and erythrocyte phenotypes of patients with mutations inheritance in PIEZO1, Spectrin ß1, RhAG and SLC4A1Blood Cells, Molecules and Diseases, 2023, pp.102780. ⟨10.1016/j.bcmd.2023.102780⟩
Article dans une revue
hal-04166631v1
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Hereditary spherocytosis associated with Noonan syndrome mimicking a dyserythropoietic anaemiaPediatric Blood and Cancer, 2022, ⟨10.1002/pbc.30121⟩
Article dans une revue
hal-03925663v1
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