Isochromosome 7p, i(7)(p10): A rare AML, myelodysplasia-related entity

We describe genomic findings in an AML case with isochromosome 7p, i(7)(p10), in which SNP array analysis uncovered an additional 7.07-Mb 20q deletion not detected by karyotyping. Several AML cases with i(7)(p10) as an isolated cytogenetic finding have been previously reported. Based on consequent l...

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Detalles Bibliográficos
Autores principales: Nejati, Reza, Neumann-Domer, Ryan, Liu, Zemin, Koslosky, Lori, Neumann-Domer, Erin, Pei, Jianming, Wang, Y. Lynn, Testa, Joseph R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493252/
https://www.ncbi.nlm.nih.gov/pubmed/37701905
http://dx.doi.org/10.1016/j.lrr.2023.100387

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493252/
https://www.ncbi.nlm.nih.gov/pubmed/37701905
http://dx.doi.org/10.1016/j.lrr.2023.100387

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