1. Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders. Issue 1 (December 2016) Authors: Latger-Cannard, Veronique; Philippe, Christophe; Bouquet, Alexandre; Baccini, Veronique; Alessi, Marie-Christine; Ankri, Annick; Bauters, Anne; Bayart, Sophie; Cornillet-Lefebvre, Pascale; Daliphard, Sylvie; Mozziconacci, Marie-Joelle; Renneville, Aline; Ballerini, Paola; Leverger, Guy; Sobol, Ha... Journal: Orphanet journal of rare diseases Issue: Volume 11:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗