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t(1;7;22)(p13;q21;q13) is a novel 3-way variant of t(1;22)(p13;q13) neonatal acute megakaryoblastic leukemia: A case report

Acute megakaryoblastic leukemia (AMKL) is a rare disease, occurring mostly in infants and young children. The chromosomal translocation t(1;22)(p13;q13), resulting in the RBM15-MKL1 fusion gene, is a recurrent and diagnostic translocation in infants with AMKL. The present case report describes a cas...

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Detalles Bibliográficos
Autores principales:	Messiaen, Julie, Uyttebroeck, Anne, Michaux, Lucienne, Vandenberghe, Peter, Boeckx, Nancy, Jacobs, Sandra A.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2023
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926329/ https://www.ncbi.nlm.nih.gov/pubmed/36798463 http://dx.doi.org/10.3892/mco.2023.2614

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