Characterization of cases with the rare cytogenetic abnormality i(7)(p10) reveals an association with IDH2-mutated AML
Author:
Affiliation:
1. MLL Munich Leukemia Laboratory, Munich, Germany
Publisher
American Society of Hematology
Link
https://ashpublications.org/bloodadvances/article-pdf/8/15/4125/2238103/blooda_adv-2024-013225-main.pdf
Reference16 articles.
1. The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms;Khoury;Leukemia,2022
2. Diagnosis and management of AML in adults: 2022 recommendations from an international expert panel on behalf of the ELN;Döhner;Blood,2022
3. Isochromosome 7p, i(7)(p10): a rare AML, myelodysplasia-related entity;Nejati;Leuk Res Rep,2023
4. Mitelman F , JohanssonB, MertensF. Mitelman database of chromosome aberrations and gene fusions in cancer. Accessed 15 January 2024. https://mitelmandatabase.isb-cgc.org.
5. Morphologic dysplasia in de novo acute myeloid leukemia (AML) is related to unfavorable cytogenetics but has no independent prognostic relevance under the conditions of intensive induction therapy: results of a multiparameter analysis from the German AML Cooperative Group studies;Haferlach;J Clin Oncol,2003
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