Baseline dysmegakaryopoiesis in inherited thrombocytopenia/platelet disorder with predisposition to haematological malignancies
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Title
Baseline dysmegakaryopoiesis in inherited thrombocytopenia/platelet disorder with predisposition to haematological malignancies
Authors
Keywords
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Journal
BRITISH JOURNAL OF HAEMATOLOGY
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2020-02-27
DOI
10.1111/bjh.16543
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Note: Only part of the references are listed.- Bone Marrow Morphology Associated With Germline RUNX1 Mutations in Patients With Familial Platelet Disorder With Associated Myeloid Malignancy
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- Myelodysplastic syndromes and acute leukemia with genetic predispositions: a new challenge for hematologists
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- Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia
- (2015) I Antony-Debré et al. LEUKEMIA
- Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy
- (2015) Michael Y Zhang et al. NATURE GENETICS
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- (2015) J Perez Botero et al. Blood Cancer Journal
- Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation
- (2014) Dominique Bluteau et al. JOURNAL OF CLINICAL INVESTIGATION
- Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression
- (2012) D. Bluteau et al. BLOOD
- MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations
- (2012) I. Antony-Debre et al. BLOOD
- Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families
- (2011) P. Noris et al. BLOOD
- Dysmegakaryopoiesis, a Clue for an Early Diagnosis of Familial Platelet Disorder With Propensity to Acute Myeloid Leukemia in Case of Unexplained Inherited Thrombocytopenia Associated With Normal-sized Platelets
- (2011) Véronique Latger-Cannard et al. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
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