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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 bloodadvances.2024013225.
https://doi.org/10.1182/bloodadvances.2024013225
Published: 2024
Includes: Supplemental data