Search Results - Lüttgen, Sabine

Germline AGO2 mutations impair RNA interference and human neurological development by Lessel, Davor (Author) , Zeitler, Daniela M. (Author) , Reijnders, Margot R. F. (Author) , Kazantsev, Andriy (Author) , Hassani Nia, Fatemeh (Author) , Bartholomäus, Alexander (Author) , Martens, Victoria (Author) , Bruckmann, Astrid (Author) , Graus, Veronika (Author) , McConkie-Rosell, Allyn (Author) , McDonald, Marie (Author) , Lozic, Bernarda (Author) , Tan, Ee-Shien (Author) , Gerkes, Erica (Author) , Johannsen, Jessika (Author) , Denecke, Jonas (Author) , Telegrafi, Aida (Author) , Zonneveld-Huijssoon, Evelien (Author) , Lemmink, Henny H. (Author) , Cham, Breana W. M. (Author) , Kovacevic, Tanja (Author) , Ramsdell, Linda (Author) , Foss, Kimberly (Author) , Le Duc, Diana (Author) , Mitter, Diana (Author) , Syrbe, Steffen (Author) , Merkenschlager, Andreas (Author) , Sinnema, Margje (Author) , Panis, Bianca (Author) , Lazier, Joanna (Author) , Osmond, Matthew (Author) , Hartley, Taila (Author) , Mortreux, Jeremie (Author) , Busa, Tiffany (Author) , Missirian, Chantal (Author) , Prasun, Pankaj (Author) , Lüttgen, Sabine (Author) , Mannucci, Ilaria (Author) , Lessel, Ivana (Author) , Schob, Claudia (Author) , Kindler, Stefan (Author) , Pappas, John (Author) , Rabin, Rachel (Author) , Willemsen, Marjolein (Author) , Gardeitchik, Thatjana (Author) , Löhner, Katharina (Author) , Rump, Patrick (Author) , Dias, Kerith-Rae (Author) , Evans, Carey-Anne (Author) , Andrews, Peter Ian (Author) , Roscioli, Tony (Author) , Brunner, Han G. (Author) , Chijiwa, Chieko (Author) , Lewis, M. E. Suzanne (Author) , Abou Jamra, Rami (Author) , Dyment, David A. (Author) , Boycott, Kym M. (Author) , Stegmann, Alexander P. A. (Author) , Kubisch, Christian (Author) , Tan, Ene-Choo (Author) , Mirzaa, Ghayda M. (Author) , McWalter, Kirsty (Author) , Kleefstra, Tjitske (Author) , Pfundt, Rolph (Author) , Ignatova, Zoya (Author) , Meister, Gunter (Author) , Kreienkamp, Hans-Jürgen (Author) ,

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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) ,

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