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Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders.
Latger-Cannard V, Philippe C, Bouquet A, Baccini V, Alessi MC, Ankri A, Bauters A, Bayart S, Cornillet-Lefebvre P, Daliphard S, Mozziconacci MJ, Renneville A, Ballerini P, Leverger G, Sobol H, Jonveaux P, Preudhomme C, Nurden P, Lecompte T, Favier R. Latger-Cannard V, et al. Orphanet J Rare Dis. 2016 Apr 26;11:49. doi: 10.1186/s13023-016-0432-0. Orphanet J Rare Dis. 2016. PMID: 27112265 Free PMC article.
[Thrombocytopenia: clinicobiologic validation and classification].
Latger-Cannard V, Salignac S, Salmon A, Mansuy L, de Maistre E, Botte C, Bordigoni P, Schlegel N, Lecompte T. Latger-Cannard V, et al. Ann Biol Clin (Paris). 2005 Nov-Dec;63(6):599-610. Ann Biol Clin (Paris). 2005. PMID: 16330378 Free article. Review. French.
[Platelets satellitism with polynuclear neutrophils].
Dauendorffer JN, Latger-Cannard V, Lesesvre JF, Lecompte T. Dauendorffer JN, et al. Ann Biol Clin (Paris). 2000 Jan-Feb;58(1):91-3. Ann Biol Clin (Paris). 2000. PMID: 10673619 Free article. French. No abstract available.
90 results