Search Results - Zirn, Birgit

FOXG1 syndrome: genotype–phenotype association in 83 patients with FOXG1 variants by Mitter, Diana (Author) , Pringsheim, Milka (Author) , Kaulisch, Marc (Author) , Plümacher, Kim Sarah (Author) , Schröder, Simone (Author) , Warthemann, Rita (Author) , Abou Jamra, Rami (Author) , Baethmann, Martina (Author) , Bast, Thomas (Author) , Büttel, Hans-Martin (Author) , Cohen, Julie S. (Author) , Conover, Elizabeth (Author) , Courage, Carolina (Author) , Eger, Angelika (Author) , Fatemi, Ali (Author) , Grebe, Theresa A. (Author) , Hauser, Natalie S. (Author) , Heinritz, Wolfram (Author) , Helbig, Katherine L. (Author) , Heruth, Marion (Author) , Huhle, Dagmar (Author) , Höft, Karen (Author) , Karch, Stephanie (Author) , Kluger, Gerhard (Author) , Korenke, Christoph (Author) , Lemke, Johannes R. (Author) , Lutz, Richard E. (Author) , Patzer, Steffi (Author) , Prehl, Isabelle (Author) , Hoertnagel, Konstanze (Author) , Ramsey, Keri (Author) , Rating, Tina (Author) , Rieß, Angelika (Author) , Rohena, Luis (Author) , Schimmel, Mareike (Author) , Westman, Rachel (Author) , Zech, Frank-Martin (Author) , Zoll, Barbara (Author) , Malzahn, Dörthe (Author) , Zirn, Birgit (Author) , Brockmann, Knut (Author) ,

• Resolving-System, kostenfrei, Volltext

Phenotypic spectrum associated with CASK loss-of-function mutations by Moog, Ute (Author) , Kutsche, Kerstin (Author) , Kortüm, Fanny (Author) , Chilian, Bettina (Author) , Bierhals, Tatjana (Author) , Apeshiotis, Neophytos (Author) , Balg, Stefanie (Author) , Chassaing, Nicolas (Author) , Coubes, Christine (Author) , Das, Soma (Author) , Engels, Hartmut (Author) , Esch, Hilde Van (Author) , Grasshoff, Ute (Author) , Heise, Marisol (Author) , Isidor, Bertrand (Author) , Jarvis, Joanna (Author) , Koehler, Udo (Author) , Martin, Thomas (Author) , Oehl-Jaschkowitz, Barbara (Author) , Ortibus, Els (Author) , Pilz, Daniela T. (Author) , Prabhakar, Prab (Author) , Rappold, Gudrun (Author) , Rau, Isabella (Author) , Rettenberger, Günther (Author) , Schlüter, Gregor (Author) , Scott, Richard H. (Author) , Shoukier, Moonef (Author) , Wohlleber, Eva (Author) , Zirn, Birgit (Author) , Dobyns, William B. (Author) , Uyanik, Gökhan (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Phenotypic spectrum associated with CASK loss-of-function mutations by Moog, Ute (Author) , Kutsche, Kerstin (Author) , Kortüm, Fanny (Author) , Chilian, Bettina (Author) , Bierhals, Tatjana (Author) , Apeshiotis, Neophytos (Author) , Balg, Stefanie (Author) , Chassaing, Nicolas (Author) , Coubes, Christine (Author) , Das, Soma (Author) , Engels, Hartmut (Author) , Esch, Hilde Van (Author) , Grasshoff, Ute (Author) , Heise, Marisol (Author) , Isidor, Bertrand (Author) , Jarvis, Joanna (Author) , Koehler, Udo (Author) , Martin, Thomas (Author) , Oehl-Jaschkowitz, Barbara (Author) , Ortibus, Els (Author) , Pilz, Daniela T. (Author) , Prabhakar, Prab (Author) , Rappold, Gudrun (Author) , Rau, Isabella (Author) , Rettenberger, Günther (Author) , Schlüter, Gregor (Author) , Scott, Richard H. (Author) , Shoukier, Moonef (Author) , Wohlleber, Eva (Author) , Zirn, Birgit (Author) , Dobyns, William B. (Author) , Uyanik, Gökhan (Author) ,