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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Egile Nagusiak:	Reza Nejati, Ryan Neumann-Domer, Zemin Liu, Lori Koslosky, Erin Neumann-Domer, Jianming Pei, Y. Lynn Wang, Joseph R. Testa
Formatua:	Artigo
Hizkuntza:	Inglês
Argitaratua:	Elsevier 2023-01-01
Saila:	Leukemia Research Reports
Gaiak:	Acute myeloid leukemia i(7p) 7q deletion 20q deletion Chromosome microarray analysis Mutations
Sarrera elektronikoa:	http://www.sciencedirect.com/science/article/pii/S2213048923000274
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