Entries of Schmitt, Wolfgang on the publication server

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 and 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), pp. 445-452. Fulltext not available.

Wieczorek, Dagmar, Shaw‐Smith, Charles, Kohlhase, Jürgen, Schmitt, Wolfgang, Buiting, Karin, Coffey, Alison, Howard, Eleanor, Hehr, Ute and 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), pp. 1135-1142. Fulltext not available.

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 and 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), pp. 138-146. Fulltext not available.