Germline RUNX1 Intragenic Deletion: Implications for Accurate Diagnosis of FPD/AML-Reference-Cited by-同舟云学术

Germline RUNX1 Intragenic Deletion: Implications for Accurate Diagnosis of FPD/AML

Published:2019-04-02 Issue:3 Volume:3 Page:e203
ISSN:2572-9241
Container-title:HemaSphere
language:en
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Author:

Duployez Nicolas,Martin Jean-Edouard,Khalife-Hachem Sabine,Benkhelil Ryane,Saada Véronique,Marzac Christophe,Auger Nathalie,Marceau-Renaut Alice,Favier Rémi,Ballerini Paola,Caron Olivier,Baruchel André,de Botton Stéphane,Preudhomme Claude,Micol Jean-Baptiste,Raslova Hana,Antony-Debré Iléana

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology

Reference15 articles.

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2. Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia;Antony-Debre;Leukemia.,2016

3. High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder;Preudhomme;Blood.,2009

4. Level of RUNX1 activity is critical for leukemic predisposition but not for thrombocytopenia;Antony-Debre;Blood.,2015

5. Familial platelet disorder with predisposition to acute myelogenous leukemia;Heller;Atlas Genet Cytogenet Oncol Haematol.,2013

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