Einträge von Schmitt, Wolfgang auf dem Publikationsserver

Behrens, Angelika, Kreuzmayr, Anton, Manner, Hendrik, Koop, Herbert, Lorenz, Albrecht, Schaefer, Claus, Plauth, Mathais, Jetschmann, Jens-Uwe, von Tirpitz, Christian, Ewald, Marcus, Sackmann, Michael, Renner, Wanja, Krüger, Martin, Schwab, Dieter, Hoffmann, Werner, Engelke, Olaf, Pech, Oliver, Kullmann, Frank, Pampuch, Sonja, Lenfers, Berthold, Weickert, Uwe, Schilling, Dieter, Boehm, Stephan, Beckebaum, Susanne, Cicinnati, Vito, Erckenbrecht, Joachim F., Dumoulin, Franz Ludwig, Benz, Claus, Rabenstein, Thomas, Haltern, Georg, Balsliemke, Martin, de Mas, Christian, Kleber, Gerhard, Pehl, Christian, Vogt, Christoph, Kiesslich, Ralf, Fischbach, Wolfgang, Koop, Irmtraut, Kuehne, Jens, Breidert, Matthias, Sass, Nils Lennart, May, Andrea, Friedrich, Christian, Veitt, Ronni, Porschen, Rainer, Ellrichmann, Mark, Arlt, Alexander, Schmitt, Wolfgang, Dollhopf, Markus, Schmidbaur, Werner, Dignass, Axel, Schmitz, Volker, Labenz, J., Kaiser, Gernot, Krannich, Alexander, Barteska, Nico und Ell, Christian (2018) Acute sedation-associated complications in GI endoscopy (ProSed 2 Study): results from the prospective multicentre electronic registry of sedation-associated complications. Gut 68 (3), S. 445-452. Volltext nicht vorhanden.

Wieczorek, Dagmar, Shaw‐Smith, Charles, Kohlhase, Jürgen, Schmitt, Wolfgang, Buiting, Karin, Coffey, Alison, Howard, Eleanor, Hehr, Ute und Gillessen‐Kaesbach, Gabriele (2007) Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup‐shaped ears, congenital heart defect, and mental retardation—New MCA/MR syndrome in two affected sibs and a mildly affected mother? American Journal of Medical Genetics Part A 143A (11), S. 1135-1142. Volltext nicht vorhanden.

Grabowski, Monika, Mueller-Koch, Yvonne, Grasbon-Frodl, Eva, Koehler, Udo, Keller, Gisela, Vogelsang, Holger, Dietmaier, Wolfgang, Kopp, Reinhard, Siebers, Ulrike, Schmitt, Wolfgang, Neitzel, Birgit, Gruber, Maria, Doerner, Christa, Kerker, Brigitte, Ruemmele, Petra, Henke, Gabriele und Holinski-Feder, Elke (2005) Deletions Account for 17% of Pathogenic Germline Alterations in MLH1 and MSH2 in Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Families. Genetic Testing 9 (2), S. 138-146. Volltext nicht vorhanden.