C. Senger

Type 2 NF1 deletions are highly unusual by virtue of the absence of nonallelic homologous recombination hotspots and an apparent preference for female mitotic recombination.

D. Cooper, C. Lázaro, H. Kehrer-Sawatzki, 2007, American journal of human genetics.

Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis

K Holzmann, I. Radtke, L. Bullinger, 2010, Leukemia.