Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders-Reference-Cited by-同舟云学术

Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders

Published:2016-04-26 Issue:1 Volume:11 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

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 Hagay,Jonveaux Philippe,Preudhomme Claude,Nurden Paquita,Lecompte Thomas,Favier Remi

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-016-0432-0

Reference37 articles.

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