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