Publikationen von Susann Schweiger

Schweiger, S.; Schneider, R.: The MID1/PP2A complex: a key to the pathogenesis of Opitz BBB/G syndrome. BioEssays 25 (4), S. 356 - 366 (2003)

Schweiger, S.; Chaoui, R.; Tennstedt, C.; Lehmann, K.; Mundlos, S.; Tinschert, S.: Antenatal onset of cortical hyperostosis (Caffey disease): Case report and review. American Journal of Medical Genetics Part A 120A (4), S. 547 - 552 (2003)

Winter, J.; Lehmann, T.; Suckow, V.; Kijas, Z.; Kulozik, A.; Kalscheuer, V.; Hamel, B.; Devriendt, K.; Opitz, J.; Lenzner, S. et al.; Ropers, H.-H.; Schweiger, S.: Duplication of the MID1 first exon in a patient with Opitz G/BBB syndrome. Human Genetics 112 (3), S. 249 - 254 (2003)

Musante, L.; Kehl, H. G.; Majewski, F.; Meinecke, P.; Schweiger, S.; Gillessen-Kaesbach, G.; Wieczorek, D.; Hinkel, G. K.; Tinschert, S.; Hoeltzenbein, M. et al.; Ropers, H.-H.; Kalscheuer, V. M.: Spectrum of mutations in PTPN11 and genotype-phenotype correlation in 96 patients with Noonan syndrome and five patients with cardio-facio-cutanesous syndrome. European Journal of Human Genetics 11 (2), S. 201 - 206 (2003)

Raderschall, E.; Stout, K.; Freier, S.; Suckow, V.; Schweiger, S.; Haaf, T.: Elevated Levels of Rad51 Recombination Protein in Tumor Cells. Cancer Research 62 (1), S. 219 - 225 (2002)