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authFullName_s : Odile Fenneteau

GATA-1 Defects in Diamond-Blackfan Anemia: Phenotypic Characterization Points to a Specific Subset of Disease

Birgit Van Dooijeweert , Sima Kheradmand Kia , Niklas Dahl , Odile Fenneteau , Roos Leguit , et al.
Genes, 2022, 13 (3), ⟨10.3390/genes13030447⟩
Article dans une revue hal-03641414v1

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 SLC4A1

Benoit Allegrini , Ludivine David Nguyen , Morgane Mignotet , Catherine Etchebest , Odile Fenneteau , et al.
Blood Cells, Molecules and Diseases, 2023, pp.102780. ⟨10.1016/j.bcmd.2023.102780⟩
Article dans une revue hal-04166631v1

Hereditary spherocytosis associated with Noonan syndrome mimicking a dyserythropoietic anaemia

Sarah Faggetter , Alina Ferster , Laurence Dedeken , Anne Demulder , Ludvine David-Nguyen , et al.
Pediatric Blood and Cancer, 2022, ⟨10.1002/pbc.30121⟩
Article dans une revue hal-03925663v1