Identification and molecular characterization of a novel 3′ mutation inRUNX1in a family with familial platelet disorder
Author:
Publisher
Informa UK Limited
Subject
Cancer Research,Oncology,Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/10428194.2010.503821
Reference15 articles.
1. Evidence for Genetic Homogeneity in a Familial Platelet Disorder With Predisposition to Acute Myelogenous Leukemia (FPD/AML)
2. Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardation
3. Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions
4. A novel CBFA2 single-nucleotide mutation in familial platelet disorder with propensity to develop myeloid malignancies
5. A novel RUNX1 mutation in familial platelet disorder with propensity to develop myeloid malignancies
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