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Article

Evidence for genetic homogeneity in a familial platelet disorder with predisposition to acute myelogenous leukemia (FPD/AML)

Blood - 1 Oct 1998

Arepally G, Rebbeck T R, Song W, Gilliland G, Maris J M, Poncz M

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 9746808

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Related research

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Evidence for genetic homogeneity in a familial platelet disorder with predisposition to acute myelogenous leukemia (FPD/AML)PMID 9746808Read ↗

Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemiaSemantic proximity Read ↗

Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndromeSemantic proximity Read ↗

Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies.Semantic proximity Read ↗

Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele.Semantic proximity Read ↗

Myeloid neoplasms with germ line RUNX1 mutation.Semantic proximity Read ↗

High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorderSemantic proximity Read ↗

Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy.Semantic proximity Read ↗

Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy)Semantic proximity Read ↗

Targeted next-generation sequencing of familial platelet disorder with predisposition to acute myeloid leukaemia.Semantic proximity Read ↗

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.Semantic proximity Read ↗

A novel RUNX1 mutation in a kindred with familial platelet disorder with propensity to acute myeloid leukaemia: male predominance of affected individuals.Semantic proximity Read ↗

Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia.Semantic proximity Read ↗

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