Search Results - Udo Trautmann
- Showing 1 - 8 results of 8
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Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation by Anita Rauch, Juliane Hoyer, Sabine Guth, Christiane Zweier, Cornelia Kraus, Christian Becker, Martin Zenker, Ulrike Hüffmeier, Christian T. Thiel, Franz Rüschendorf, Peter Nürnberg, André Reis, Udo Trautmann
Published 2006Artigo -
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Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays by Juliane Hoyer, Alexander Dreweke, C. Becker, Isabel Göhring, Christian T. Thiel, Maarit Peippo, Rami Rauch, Michael Hofbeck, Udo Trautmann, Christiane Zweier, Martin Zenker, Ulrike Hüffmeier, Cornelia Kraus, Arif B. Ekici, Franz Rüschendorf, Peter Nürnberg, André Reis, Anita Rauch
Published 2007Artigo -
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Mutations in the ZNF41 Gene Are Associated with Cognitive Deficits: Identification of a New Candidate for X-Linked Mental Retardation by Sarah A. Shoichet, Kirsten Hoffmann, Corinna Menzel, Udo Trautmann, Bettina A. Moser, Maria Hoeltzenbein, Bernard Échenne, M. W. Partington, Hans van Bokhoven, Claude Moraine, Jean‐Pierre Fryns, Jamel Chelly, Hans‐Dieter Rott, Hans‐Hilger Ropers, Vera M. Kalscheuer
Published 2003Artigo -
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Need for high-resolution Genetic Analysis in iPSC: Results and Lessons from the ForIPS Consortium by Bernt Popp, Mandy Krumbiegel, Janina Grosch, Annika Sommer, Steffen Uebe, Zacharias Kohl, Sonja Plötz, Michaela Farrell, Udo Trautmann, Cornelia Kraus, Arif B. Ekici, Reza Asadollahi, Martin Regensburger, Katharina Günther, Anita Rauch, Frank Edenhofer, Jürgen Winkler, Beate Winner, André Reis
Published 2018Artigo -
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Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome–like phenotype and hyperactivated MAPK signaling in humans and mice by Michael S. Kraft, Ion Cristian Cirstea, Anne K. Voss, Tim Thomas, Ina Goehring, Bilal N. Sheikh, Lavinia Gordon, Hamish S. Scott, Gordon K. Smyth, Mohammad Reza Ahmadian, Udo Trautmann, Martin Zenker, Marco Tartaglia, Arif B. Ekici, André Reis, Helmuth-Guenther Dörr, Anita Rauch, Christian T. Thiel
Published 2011Artigo -
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Genetic screening confirms heterozygous mutations in ACAN as a major cause of idiopathic short stature by Nadine Hauer, Heinrich Sticht, Sangamitra Boppudi, Christian Büttner, Cornelia Kraus, Udo Trautmann, Martin Zenker, Christiane Zweier, Antje Wiesener, Rami Abou Jamra, Dagmar Wieczorek, Jaqueline Kelkel, Anna‐Maria Jung, Steffen Uebe, Arif B. Ekici, Tilman Rohrer, André Reis, Helmuth‐Günther Dörr, Christian T. Thiel
Published 2017Artigo -
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Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature by Nadine Hauer, Bernt Popp, Schoeller Eva, Sarah Schuhmann, Karen E. Heath, Alfonso Hisado-Oliva, Patricia Klinger, Cornelia Kraus, Udo Trautmann, Martin Zenker, Christiane Zweier, Antje Wiesener, Rami Abou Jamra, Erdmute Kunstmann, Dagmar Wieczorek, Steffen Uebe, Fulvia Ferrazzi, Christian Büttner, Arif B. Ekici, Anita Rauch, Heinrich Sticht, Helmuth‐Günther Dörr, André Reis, Christian T. Thiel
Published 2017Artigo
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