Figure 2
Figure 2. Frequency and distribution of cytogenetic abnormalities in patients exhibiting at least one abnormality. Excluding the WHO category “AML with recurrent genetic abnormalities”1 (A, t-AML n = 78, B, de novo AML, n = 698; definition “complex” according to Döhner et al28 and of “monosomal karyotype” according to Breems et al40).

Frequency and distribution of cytogenetic abnormalities in patients exhibiting at least one abnormality. Excluding the WHO category “AML with recurrent genetic abnormalities”1  (A, t-AML n = 78, B, de novo AML, n = 698; definition “complex” according to Döhner et al28  and of “monosomal karyotype” according to Breems et al40 ).

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