inv(11)(q13q23) KMT2A/BTBD18
KMT2A - Wikipedia
The EGR3 regulome of infant KMT2A-r acute lymphoblastic leukemia identifies differential expression of B-lineage genes predictive for outcome | Cancer Community
Human MLL/KMT2A gene exhibits a second breakpoint cluster region for recurrent MLL–USP2 fusions | Leukemia
Human MLL/KMT2A gene exhibits a second breakpoint cluster region for recurrent MLL–USP2 fusions | Leukemia
XL KMT2A BA - Break Apart Probe | MetaSystems Probes
Biomedicines | Free Full-Text | BTK, NUTM2A, and PRPF19 Are Novel KMT2A Partner Genes in Childhood Acute Leukemia
KMT2A-MLLT4 Dual Fusion/Translocation FISH Probe Kit - CytoTest
KMT2A (myeloid/lymphoid or mixed lineage leukemia)
Rare KMT2A-ELL and Novel ZNF56-KMT2A Fusion Genes in Pediatric T-cell Acute Lymphoblastic Leukemia | Cancer Genomics & Proteomics
Montreal Biotech kmt2a-mll-gene-break-apart-detection-probe-mll
Genes | Free Full-Text | KMT2A: Umbrella Gene for Multiple Diseases
Biomedicines | Free Full-Text | Updates in KMT2A Gene Rearrangement in Pediatric Acute Lymphoblastic Leukemia
Biomedicines | Free Full-Text | BTK, NUTM2A, and PRPF19 Are Novel KMT2A Partner Genes in Childhood Acute Leukemia
The KMT2A recombinome of acute leukemias in 2023 | Leukemia
CytoCell MLL (KMT2A) Breakapart FISH Probe | OGT
XL MLL plus - Break Apart Probe | MetaSystems Probes
KMT2A - Wikipedia
Frontiers | Drug Repurposing for Targeting Acute Leukemia With KMT2A (MLL)— Gene Rearrangements
A. Location of reported KMT2A mutation: Electrophogram of egi 9 of the... | Download Scientific Diagram
KMT2A and KMT2B Mediate Memory Function by Affecting Distinct Genomic Regions - ScienceDirect
Schematic for the pathogenesis of MLL. As described in Box 2, both... | Download Scientific Diagram
Frontiers | MLL-Rearranged Leukemias—An Update on Science and Clinical Approaches
A novel deletion mutation in KMT2A identified in a child with ID/DD and blood eosinophilia | BMC Medical Genetics | Full Text
Molecular and cellular issues of KMT2A variants involved in Wiedemann-Steiner syndrome | European Journal of Human Genetics
