Characterization of TCF3 rearrangements in pediatric B-lymphoblastic leukemia/lymphoma by mate-pair sequencing (MPseq) identifies complex genomic rearrangements and a novel TCF3/TEF gene fusion

The TCF3/PBX1 gene fusion is a recurrent genetic abnormality in pediatric B-lymphoblastic leukemia/lymphoma (B-ALL/LBL). While dual-color, dual-fusion fluorescence in situ hybridization (D-FISH) probes can detect TCF3/PBX1 fusions, further characterization of atypical TCF3 FISH patterns as indicated...

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Vydáno v:Blood Cancer J
Hlavní autoři: Rowsey, Ross A., Smoley, Stephanie A., Williamson, Cynthia M., Vasmatzis, George, Smadbeck, James B., Ning, Yi, Greipp, Patricia T., Hoppman, Nicole L., Baughn, Linda B., Ketterling, Rhett P., Peterson, Jess F.
Médium: Artigo
Jazyk:Inglês
Vydáno: Nature Publishing Group UK 2019
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6773761/
https://ncbi.nlm.nih.gov/pubmed/31575852
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41408-019-0239-z
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