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Article

Childhood B-cell precursor acute lymphoblastic leukaemia in a patient with familial thrombocytopenia and RUNX1 mutation.

British journal of haematology - 1 Dec 2010

Linden Tobias, Schnittger Susanne, Groll Andreas H, Juergens Heribert, Rossig Claudia

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Share to Child, Preschool
Share to Core Binding Factor Alpha 2 Subunit
Share to RUNX1 gene
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Precursor Cell Lymphoblastic Leukemia-Lymphoma

Share to Thrombocytopenia

Source

Identifiers

PMID: 20880108
DOI: 10.1111/j.1365-2141.2010.08370.x

Genes

RUNX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Childhood B-cell precursor acute lymphoblastic leukaemia in a patient with familial thrombocytopenia and RUNX1 mutation.PMID 20880108Read ↗

B-cell acute lymphoblastic leukemia in patients with germline RUNX1 mutations.Semantic proximity Read ↗

A novel inherited mutation of the transcription factor RUNX1 causes thrombocytopenia and may predispose to acute myeloid leukaemia.Semantic proximity Read ↗

A unique presentation of T-lymphoblastic lymphoma in a pediatric patient with a germline RUNX1 mutation.Semantic proximity Read ↗

A de novo germline RUNX1 variant preceding development of concurrent T-lymphoblastic leukemia and myelodysplastic syndrome.Semantic proximity Read ↗

Recent developments in the management of T-cell precursor acute lymphoblastic leukemia/lymphoma.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 ↗

Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopenia.Semantic proximity Read ↗

Germline PAX5 mutation predisposes to familial B-cell precursor acute lymphoblastic leukemia.Semantic proximity Read ↗

B-cell acute lymphoblastic leukemia and juvenile xanthogranuloma in a patient with ETV6 thrombocytopenia and leukemia predisposition syndrome: novel clinical presentation and perspective.Semantic proximity Read ↗

Novel activating STAT5B mutations as putative drivers of T-cell acute lymphoblastic leukemia.Semantic 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 ↗

Distinctive phenotypes in two children with novel germline RUNX1 mutations - one with myeloid malignancy and increased fetal hemoglobin.Semantic proximity Read ↗

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