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Publications by Zenker, Martin

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Number of items: 5.

Journal article

Ripperger, Tim; Bielack, Stefan S.; Borkhardt, Arndt; Brecht, Ines B.; Burkhardt, Birgit; Calaminus, Gabriele; Debatin, Klaus-Michael; Deubzer, Hedwig; Dirksen, Uta; Eckert, Cornelia; Eggert, Angelika; Erlacher, Miriam; Fleischhack, Gudrun; Frühwald, Michael C.; Gnekow, Astrid; Göhring, Gudrun; Graf, Norbert; Hanenberg, Helmut; Hauer, Julia; Hero, Barbara; Hettmer, Simone; Hoff, Katja von; Horstmann, Martin; Hoyer, Juliane; Illig, Thomas; Kaatsch, Peter; Kappler, Roland; Kerl, Kornelius; Klingebiel, Thomas; Kontny, Udo; Kordes, Uwe; Körholz, Dieter; Koscielniak, Ewa; Kramm, Christof M.; Kuhlen, Michaela; Kulozik, Andreas E.; Lamottke, Britta; Leuschner, Ivo; Lohmann, Dietmar R.; Meinhardt, Andrea; Metzler, Markus; Meyer, Lüder H.; Moser, Olga; Nathrath, Michaela; Niemeyer, Charlotte M.; Nustede, Rainer; Pajtler, Kristian W.; Paret, Claudia; Rasche, Mareike; Reinhardt, Dirk; Riess, Olaf; Russo, Alexandra; Rutkowski, Stefan; Schlegelberger, Brigitte; Schneider, Dominik; Schneppenheim, Reinhard; Schrappe, Martin; Schröder, Christopher; Schweinitz, Dietrich von; Simon, Thorsten; Sparber-Sauer, Monika; Spix, Claudia; Stanulla, Martin; Steinemann, Doris; Strahm, Brigitte; Temming, Petra; Thomay, Kathrin; Bueren, Andre O. von; Vorwerk, Peter; Witt, Olaf; Wlodarski, Marcin; Wössmann, Willy; Zenker, Martin; Zimmermann, Stefanie; Pfister, Stefan M.; Kratz, Christian P. (2017): Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology. In: American Journal of Medical Genetics Part A, Vol. 173, No. 4: pp. 1017-1037

Weber, Stefanie; Büscher, Anja K.; Hagmann, Henning; Liebau, Max C.; Heberle, Christian; Ludwig, Michael; Rath, Sabine; Alberer, Martin; Beissert, Antje; Zenker, Martin; Hoyer, Peter F.; Konrad, Martin; Klein, Hanns-Georg; Hoefele, Julia (2016): Dealing with the incidental finding of secondary variants by the example of SRNS patients undergoing targeted next-generation sequencing. In: Pediatric Nephrology, Vol. 31, No. 1: pp. 73-81

Kouz, Karim; Lissewski, Christina; Spranger, Stephanie; Mitter, Diana; Riess, Angelika; Lopez-Gonzalez, Vanesa; Lüttgen, Sabine; Aydin, Hatip; Deimling, Florian von; Evers, Christina; Hahn, Andreas; Hempel, Maja; Issa, Ulrike; Kahlert, Anne-Karin; Lieb, Adrian; Villavicencio-Lorini, Pablo; Juliana Ballesta-Martinez, Maria; Nampoothiri, Sheela; Ovens-Raeder, Angela; Puchmajerová, Alena; Satanovskij, Robin; Seidel, Heide; Unkelbach, Stephan; Zabel, Bernhard; Kutsche, Kerstin; Zenker, Martin (2016): Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation. In: Genetics in Medicine, Vol. 18, No. 12: pp. 1226-1234

Mainberger, Florian; Jung, Nikolai H.; Zenker, Martin; Wahllaender, Ute; Freudenberg, Leonie; Langer, Susanne; Berweck, Steffen; Winkler, Tobias; Straube, Andreas; Heinen, Florian; Granstroem, Sofia; Mautner, Victor-Felix; Lidzba, Karen; Mall, Volker (2013): Lovastatin improves impaired synaptic plasticity and phasic alertness in patients with neurofibromatosis type 1. In: BMC Neurology 13:131 [PDF, 525kB]

Zenker, Martin; Horn, Denise; Wieczorek, Dagmar; Allanson, Judith; Pauli, Silke; van der Burgt, Ineke; Doerr, Helmuth-Guenther; Gaspar, Harald; Hofbeck, Michael; Gillessen-Kaesbach, Gabriele; Kock, Andreas; Meinecke, Peter; Mundlos, Stefan; Nowka, Anja; Rauch, Anita; Reif, Silke; Schnakenburg, Christian von; Seidel, Heide; Wehner, Lars-Erik; Zweier, Christiane; Bauhuber, Susanne; Matejas, Verena; Kratz, Christian P.; Thomas, Christoph; Kutsche, Kerstin (2007): SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome. In: Journal of Medical Genetics, Vol. 44: pp. 651-656 [PDF, 1MB]

This list was generated on Thu Jan 28 03:30:32 2021 CET.