A Rare t(1;11)(q42;q23) Rearrangement with Trisomy 8 and Trisomy 21 in a Pediatric Acute Myeloid Leukemia Patient with Aberrant CD7 Expression and Jacob Syndrome: Diagnostic Value of Conventional Cytogenetics and Fluorescence in Situ Hybridization in a Rapidly Fatal Case
J Assoc Genet Technol. 2026;52(3):80-83. ABSTRACT Acute myeloid leukemia (AML) with KMT2A gene rearrangements has been observed to demonstrate an aggressive biological behavior, especially in …