Publikationen von 0000-0003-1438-2081
(ORCID: 0000-0003-1438-2081)

Kortüm, Fanny, Das, Soma, Flindt, Max, Uyanik, Gökhan , make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference und make_name_string expected hash reference (2011) The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. Journal of Medical Genetics 48, S. 396-406.

Najm, Juliane, Horn, Denise, Wimplinger, Isabella, Golden, Jeffrey A, Chizhikov, Victor V, Sudi, Jyotsna, Christian, Susan L, Ullmann, Reinhard, Kuechler, Alma, Haas, Carola A, Flubacher, Armin, Charnas, Lawrence R, Uyanik, Gökhan, Frank, Ulrich, Klopocki, Eva , Dobyns, William B und Kutsche, Kerstin (2008) Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum. Nature Genetics 40 (9), S. 1065-1067. Volltext nicht vorhanden.

Dahl, E, Wiesmann, F, Woenckhaus, M, Stoehr, R, Wild, P J, Veeck, J , Knüchel, R, Klopocki, E , Sauter, G, Simon, R, Wieland, W F, Walter, B, Denzinger, S, Hartmann, A und Hammerschmied, C G (2007) Frequent loss of SFRP1 expression in multiple human solid tumours: association with aberrant promoter methylation in renal cell carcinoma. Oncogene 26 (38), S. 5680-5691. Volltext nicht vorhanden.

Stoehr, Robert, Wissmann, Christoph, Suzuki, Hiromu, Knuechel, Ruth, Krieg, Rene C., Klopocki, Eva , Dahl, Edgar, Wild, Peter, Blaszyk, Hagen, Sauter, Guido, Simon, Ronald , Schmitt, Ruediger, Zaak, Dirk, Hofstaedter, Ferdinand, Rosenthal, Andre, Baylin, Stephen B., Pilarsky, Christian und Hartmann, Arndt (2004) Deletions of chromosome 8p and loss of sFRP1 expression are progression markers of papillary bladder cancer. Laboratory investigation 84 (4), S. 465-478. Volltext nicht vorhanden.