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Article

Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardation.

Leukemia research - 1 Jan 2010

van der Crabben Saskia, van Binsbergen Ellen, Ausems Margreet, Poot Martin, Bierings Marc, Buijs Arjan

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Share to Child, Preschool
Share to Chromosomes, Human, Pair 21
Share to Core Binding Factor Alpha 2 Subunit

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 19679353
DOI: 10.1016/j.leukres.2009.06.030

Genes

ITSN1
RUNX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardation.PMID 19679353Read ↗

Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions.Semantic proximity Read ↗

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RUN(X) out of blood: emerging RUNX1 functions beyond hematopoiesis and links to Down syndromeSemantic proximity Read ↗

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