Items where Author is "Moog, Ute"
Article
Moog, Ute ; Bierhals, Tatjana ; Brand, Kristina ; Bautsch, Jan ; Biskup, Saskia ; Brune, Thomas ; Denecke, Jonas ; de Die-Smulders, Christine E. ; Evers, Christina ; Hempel, Maja ; Henneke, Marco ; Yntema, Helger ; Menten, Björn ; Pietz, Joachim ; Pfundt, Rolph ; Schmidtke, Jörg ; Steinemann, Doris ; Stumpel, Constance T. ; Van Maldergem, Lionel ; Kutsche, Kerstin (2015) Phenotypic and molecular insights into CASK-related disorders in males. Orphanet Journal of Rare Diseases, 10 (44). pp. 1-20. ISSN 1750-1172
van Rahden, Vanessa A. ; Rau, Isabella ; Fuchs, Sigrid ; Kosyna, Friederike K. ; Larangeira de Almeida Jr, Hiram ; Fryssira, Helen ; Isidor, Bertrand ; Jauch, Anna ; Joubert, Madeleine ; Lachmeijer, Augusta M. A. ; Zweier, Christiane ; Moog, Ute ; Kutsche, Kerstin (2014) Clinical spectrum of females with HCCS mutation: from no clinical signs to a neonatal lethal form of the microphthalmia with linear skin defects (MLS) syndrome. Orphanet journal of rare diseases, 9 (53). pp. 1-13. ISSN 1750-1172
Freunscht, Inga ; Popp, Bernt ; Blank, Rainer ; Endele, Sabine ; Moog, Ute ; Petri, Holger ; Prott, Eva-Christina ; Reis, Andre ; Rübo, Jochen ; Zabel, Bernhard ; Zenker, Martin ; Hebebrand, Johannes ; Wieczorek, Dagmar (2013) Behavioral phenotype in five individuals with de novo mutations within the GRIN2B gene. Behavioral and Brain Functions, 9 (20). pp. 1-11. ISSN 1744-9081