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Katharina Hörst
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Journal Articles

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

Anna Stengel, Katharina Hörst, Constanze Kühn, Manja Meggendorfer, Wolfgang Kern, Torsten Haferlach, Claudia Haferlach
Journal: Blood Advances
Blood Adv (2024) 8 (15): 4125–4128.
https://doi.org/10.1182/bloodadvances.2024013225
Published: 2024
Includes: Supplemental data