Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions
Mylène Béri‐Dexheimer(Centre Hospitalier Régional et Universitaire de Nancy), Philippe Jonveaux(Inserm), Bruno Leheup(Hôpital d'Enfants), Thomas Lecompte(Centre Hospitalier Régional et Universitaire de Nancy), Céline Bonnet(Inserm), Virginie Roth(Centre Hospitalier Régional et Universitaire de Nancy), Pascal Chambon(Université de Pau et des Pays de l'Adour), Marie‐José Gregoire(Centre Hospitalier Régional et Universitaire de Nancy), Véronique Latger‐Cannard(Inserm), Pierre Bordigoni(Hôpital d'Enfants), Christophe Philippe(Inserm)
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