Karl Mehnert

The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions

Hildegard Kehrer‐Sawatzki, J Häussler, W. Krone et al. · Human Genetics · 1997 · 86 citations

Medicine, Neurology, Pathology +6

16p11.2–p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2

John Barber, Victoria L. Hall, Viv Maloney et al. · European Journal of Human Genetics · 2012 · 74 citations

Life Sciences, Genetics, Molecular Genetics +16

Chromosome instability and X‐ray hypersensitivity in a microcephalic and growth‐retarded child

Gotthold Barbi, J. M. J. C. Scheres, Detlev Schindler et al. · American Journal of Medical Genetics · 1991 · 57 citations

Life Sciences, Genetics, Pediatrics +15

Mitotic Stability of Small Supernumerary Marker Chromosomes: A Study Based on 93 Immortalized Cell Lines

Hannes Spittel, Florian Kubek, Katharina Kreskowski et al. · Cytogenetic and Genome Research · 2014 · 45 citations · Full text

Life Sciences, Cell Biology, Genetics +15

Differences in the induction of SCEs between human whole blood cultures and purified lymphocyte cultures and the effect of an S9 mix

Karl Mehnert, Richard Düring, Walther Vogel et al. · Mutation Research/Environmental Mutagenesis and Related Subjects · 1984 · 38 citations

Life Sciences, Hematology, Immunology +5