Author

Kateryna Konrat

Institution: Charité – Universitätsmedizin Berlin

Observed institution: Charité – Universitätsmedizin Berlin

OpenAlex ID: A5014862285

Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotype

2010 · Véronique Dutrannoy, Ilja Demuth, et al. · Human Mutation · 33

High-throughput sequencing of microdissected chromosomal regions

2009 · Anja Weise, Bernd Timmermann, et al. · European Journal of Human Genetics · 27

Interstitial deletion 2p11.2–p12: Report of a patient with mental retardation and review of the literature

2009 · Andreas Tzschach, Luitgard M. Graul‐Neumann, et al. · American Journal of Medical Genetics Part A · 14

Works count: 3

Citation count: 74

H-index: 3

I10-index: 3