A novel RUNX1 mutation in a kindred with familial platelet disorder with propensity to acute myeloid leukaemia: male predominance of affected individuals
- 28 October 2010
- journal article
- Published by Wiley in European Journal of Haematology
- Vol. 85 (6), 552-553
- https://doi.org/10.1111/j.1600-0609.2010.01513.x
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardationLeukemia Research, 2010
- Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndromeLeukemia, 2009
- High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorderBlood, 2009
- A novel pedigree with heterozygous germline RUNX1 mutation causing familial MDS-related AML: can these families serve as a multistep model for leukemic transformation?Leukemia, 2009
- Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancyBlood, 2008
- A novel RUNX1 mutation in familial platelet disorder with propensity to develop myeloid malignanciesHaematologica, 2008
- Runx1/AML1 in Normal and Abnormal HematopoiesisInternational Journal of Hematology, 2005
- Familial platelet disorder with propensity to acute myelogenous leukemia: Genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomaliesGenes, Chromosomes and Cancer, 2004
- Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemiaNature Genetics, 1999