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Roos, A; Elbracht, M; Baudis, M; Senderek, J; Schönherr, N; Eggermann, T; Schüler, H M (2008). A 10.7 Mb interstitial deletion of 13q21 without phenotypic effect defines a further non-pathogenic euchromatic variant. American Journal of Medical Genetics. Part A, 146A(18):2417-2420.
Stahl, S; Gaetzner, S; Voss, K; Brackertz, B; Schleider, E; Sürücü, O; Kunze, E; Netzer, C; Korenke, C; Finckh, U; Habek, M; Poljakovic, Z; Elbracht, M; Rudnik-Schöneborn, S; Bertalanffy, H; Sure, U; Felbor, U (2008). Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex. Human Mutation, 29(5):709-717.