All Publications

The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.

Journal Article (4)

Journal Article
Krauß, S.; So, J.; Hambrock, M.; Köhler, A.; Kunath, M.; Scharff, C.; Wessling, M.; Grzeschik, K.-H.; Schneider, R.; Schweiger, S.: Point mutations in GLI3 lead to misregulation of its subcellular localization. PLoS ONE 4, p. e7471 - e7471 (2009)
Journal Article
Tzschach, A.; Ramel, C.; Kron, A.; Seipel, B.; Wüster, C.; Cordes, U.; Liehr, T.; Hoeltzenbein, M.; Menzel, C.; Ropers, H.-H. et al.; Ullmann, R.; Kalscheuer, V.; Decker, J.; Steinberger, D.: Hypergonadotropic hypogonadism in a patient with inv ins (2;4). International Journal of Andrology 32 (3), pp. 226 - 230 (2009)
Journal Article
Neumann, T. E.; Allanson, J.; Kavamura, I.; Kerr, B.; Neri, G.; Noonan, J.; Cordeddu, V.; Gibson, K.; Tzschach, A.; Krüger, G. et al.; Hoeltzenbein, M.; Goecke, T. O.; Kehl, H. G.; Albrecht, B.; Luczak, K.; Sasiadek, M. M.; Musante, L.; Laurie, R.; Peters, H.; Tartaglia, M.; Zenker, M.; Kalscheuer, V. M.: Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome. European Journal of Human Genetics 17 (4), pp. 420 - 425 (2009)
Journal Article
Kalscheuer, V. M.; Musante, L.; Fang, C.; Hoffmann, K.; Fuchs, C.; Carta, E.; Deas, E.; Venkateswarlu, K.; Menzel, C.; Ullmann, R. et al.; Tommerup, N.; Dalprà, L.; Tzschach, A.; Selicorni, A.; Lüscher, B.; Ropers, H.-H.; Harvey, K.; Harvey, R. J.: A balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardation. Human Mutation 30 (1), pp. 61 - 68 (2009)
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