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Article

Characterization of cases with the rare cytogenetic abnormality i(7)(p10) reveals an association with IDH2-mutated AML.

Blood advances - 13 Aug 2024

Stengel Anna, Hörst Katharina, Kühn Constanze, Meggendorfer Manja, Kern Wolfgang, Haferlach Torsten, Haferlach Claudia

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Share to Aged
Share to Chromosome Aberrations
Share to Chromosomes, Human, Pair 7
Share to Isocitrate Dehydrogenase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukemia, Myeloid, Acute

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Identifiers

PMID: 38980314
DOI: 10.1182/bloodadvances.2024013225
PMCID: PMC11345384

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

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