Varon,Raymonda

Institution: Charité-Universitätsmedizin Berlin, Germany

Top Collaborators: Neitzel H, Sperling K, Dutrannoy V, Digweed M, Demuth I, Schindler D, Gregorek H, De Sá J, Gillessen-kaesbach G, Graul-neumann LM, Lourenco CM, Radszewski J, Von Moers A, Rothe S, Schulze I, Schellenberger MT, Nicke M, Nürnberg G, Bora E, Nürnberg P

Research Interests: DNA, Families, Family, Gene, Lead, Mutations, Patient, Patients, Phenotype, Report, DNA Repair, Genes, Homologous Recombination, Nijmegen Breakage Syndrome, Phenotypes, Recombination, Sequence Analysis, Siblings, Syndrome, Ataxia