Search Results - Unkelbach, Stephan

Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation by Kouz, Karim (Author) , Lißewski, Christina (Author) , Spranger, Stephanie (Author) , Mitter, Diana (Author) , Riess, Angelika (Author) , Lopez-Gonzalez, Vanesa (Author) , Lüttgen, Sabine (Author) , Aydin, Hatip (Author) , Deimling, Florian von (Author) , Evers, Christina (Author) , Hahn, Andreas (Author) , Hempel, Maja (Author) , Issa, Ulrike (Author) , Kahlert, Anne-Karin (Author) , Lieb, Adrian (Author) , Villavicencio Lorini, Pablo (Author) , Ballesta-Martinez, Maria Juliana (Author) , Nampoothiri, Sheela (Author) , Ovens-Raeder, Angela (Author) , Puchmajerová, Alena (Author) , Satanovskij, Robin (Author) , Seidel, Heide (Author) , Unkelbach, Stephan (Author) , Zabel, Bernhard (Author) , Kutsche, Kerstin (Author) , Zenker, Martin (Author) ,

• Resolving-System, Volltext