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1. Characterization of unusual iAMP21 B‐lymphoblastic leukemia ( iAMP21‐ALL ) from the Mayo Clinic and Children's Oncology Group

2. Typical, atypical and cryptic t(15;17)(q24;q21) ( PML::RARA ) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual‐color dual‐fusion FISH studies

4. Comparative study of therapy‐related and de novo adult b‐cell acute lymphoblastic leukaemia

6. Identification of a novelKMT2A / GIMAP8gene fusion in a pediatric patient with acute undifferentiated leukemia

7. Cryptic and atypical KMT2A‐USP2 and KMT2A‐USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia

8. Clinical utility of fluorescence in situ hybridization‐based diagnosis of BCR‐ABL1 like ( P hiladelphia chromosome like) B ‐acute lymphoblastic leukemia

10. Acute leukemias harboring KMT2A/MLLT10 fusion: a 10‐year experience from a single genomics laboratory

12. Cover Image

13. Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia

14. KMT2A (MLL) rearrangements observed in pediatric/young adult T-lymphoblastic leukemia/lymphoma: A 10-year review from a single cytogenetic laboratory

16. Concomitant 11p15.4-p15.5 duplication and terminal 22q13.33 deletion in a patient with features of Beckwith-Wiedemann syndrome

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