S. Bammert

SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints

D. Cooper, C. Lázaro, J. Högel, 2014, Genome Biology.

Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions

D. Cooper, J. Högel, H. Kehrer-Sawatzki, 2010, Journal of Medical Genetics.

Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions

D. Cooper, H. Kehrer-Sawatzki, L. Kluwe, 2010, Journal of Medical Genetics.