Driver-in-the-loop Framework zur optimierten Durchfuhrung virtueller Testfahrten am Stuttgarter Fahrsimulator von Kehrer, Martin

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Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women von Sepahi, Ilnaz, Faust, Ulrike, Sturm, Marc, Bosse, Kristin, Kehrer, Martin, Heinrich, Tilman, Grundman-Hauser, Kathrin, Bauer, Peter, Ossowski, Stephan, Susak, Hana, Varon, Raymonda, Schröck, Evelin, Niederacher, Dieter, Auber, Bernd, Sutter, Christian, Arnold, Norbert, Hahnen, Eric, Dworniczak, Bernd, Wang-Gorke, Shan, Gehrig, Andrea, Weber, Bernhard H F, Engel, Christoph, Lemke, Johannes R, Hartkopf, Andreas, Nguyen, Huu Phuc, Riess, Olaf, Schroeder, Christopher

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Driver-In-the-loop Framework Zur Optimierten Durchführung Virtueller Testfahrten Am Stuttgarter Fahrsimulator von Kehrer, Martin

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Next-generation sequencing in X-linked intellectual disability von Tzschach, Andreas, Grasshoff, Ute, Beck-Woedl, Stefanie, Dufke, Claudia, Bauer, Claudia, Kehrer, Martin, Evers, Christina, Moog, Ute, Oehl-Jaschkowitz, Barbara, Di Donato, Nataliya, Maiwald, Robert, Jung, Christine, Kuechler, Alma, Schulz, Solveig, Meinecke, Peter, Spranger, Stephanie, Kohlhase, Jürgen, Seidel, Jörg, Reif, Silke, Rieger, Manuela, Riess, Angelika, Sturm, Marc, Bickmann, Julia, Schroeder, Christopher, Dufke, Andreas, Riess, Olaf, Bauer, Peter

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Next-generation sequencing in X-linked intellectual disability von Tzschach, Andreas, Grasshoff, Ute, Beck-Woedl, Stefanie, Dufke, Claudia, Bauer, Claudia, Kehrer, Martin, Evers, Christina, Moog, Ute, Oehl-Jaschkowitz, Barbara, Di Donato, Nataliya, Maiwald, Robert, Jung, Christine, Kuechler, Alma, Schulz, Solveig, Meinecke, Peter, Spranger, Stephanie, Kohlhase, Jürgen, Seidel, Jörg, Reif, Silke, Rieger, Manuela, Riess, Angelika, Sturm, Marc, Bickmann, Julia, Schroeder, Christopher, Dufke, Andreas, Riess, Olaf, Bauer, Peter

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A further case of AFG2B‐related neurodevelopmental disorder with hearing loss and microcephaly allows further clarification of pathogenicity of the variant c.1313T>C, p.(Leu438Pro)... von Grosch, Sarah, Kehrer, Martin, Riess, Olaf, Bevot, Andrea, Haack, Tobias B.

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Prenatal Multicystic Encephalomalacia Due to Anomaly of the Aortic Arch von Ehehalt, Stefan, MD, Kehrer, Martin, MD, Küker, Wilhelm, MD, Hofbeck, Michael, MD, Schöning, Martin, MD

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Pre‐ and postnatal findings in a patient with a recombinant chromosome rec(8)(qter→q21.11::p23.3→qter) due to a paternal pericentric inversion inv(8)(p23.3q21.11) and review of the... von Habhab, Wisam, Mau‐Holzmann, Ulrike, Singer, Sylke, Rieß, Angelika, Kagan, Karl‐Oliver, Gerbig, Ines, Schäferhoff, Karin, Dufke, Andreas, Kehrer, Martin

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A single center experience of prenatal parent‐fetus trio exome sequencing for pregnancies with congenital anomalies von Dufke, Andreas, Hoopmann, Markus, Waldmüller, Stephan, Prodan, Natalia Carmen, Beck‐Wödl, Stefanie, Grasshoff, Ute, Heinrich, Tilman, Riess, Angelika, Kehrer, Martin, Falb, Ruth J., Liebmann, Alexandra, Roggia, Cristiana, Stampfer, Miriam, Schadeck, Malou, Müller, Amelie J., Grimmel, Mona, Stöbe, Petra, Gauck, Darja, Buchert‐Lo, Rebecca, Baumann, Sarah, Schäferhoff, Karin, Bertrand, Miriam, Menden, Benita, Sturm, Marc, Schütz, Leon, Riess, Olaf, Ossowski, Stephan, Haack, Tobias B., Kagan, Karl Oliver

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A Longitudinal Study of Cerebral Blood Flow Over the First 30 Months von Kehrer, Martin, Schöning, Martin

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HBOC multi-gene panel testing: comparison of two sequencing centers von Schroeder, Christopher, Faust, Ulrike, Sturm, Marc, Hackmann, Karl, Grundmann, Kathrin, Harmuth, Florian, Bosse, Kristin, Kehrer, Martin, Benkert, Tanja, Klink, Barbara, Mackenroth, Luisa, Betcheva-Krajcir, Elitza, Wimberger, Pauline, Kast, Karin, Heilig, Mechthilde, Nguyen, Huu Phuc, Riess, Olaf, Schröck, Evelin, Bauer, Peter, Rump, Andreas

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Interstitial 1p32.1p32.3 deletion in a patient with multiple congenital anomalies von Kehrer, Martin, Schäferhoff, Karin, Bonin, Michael, Jauch, Anna, Bevot, Andrea, Tzschach, Andreas

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Novel HIVEP2 Variants in Patients with Intellectual Disability von Park, Joohyun, Colombo, Roberto, Schäferhoff, Karin, Janiri, Luigi, Grimmel, Mona, Sturm, Marc, Grasshoff, Ute, Dufke, Andreas, Haack, Tobias B., Kehrer, Martin

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Interstitial duplication of chromosome region 1q25.1q25.3: Report of a patient with mild cognitive deficits, tall stature and facial dysmorphisms von Kehrer, Martin, Liehr, Thomas, Benkert, Tanja, Singer, Sylke, Grasshoff, Ute, Schaeferhoff, Karin, Bonin, Michael, Weichselbaum, Annette, Tzschach, Andreas

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Development of cerebral blood flow volume in preterm neonates during the first two weeks of life von KEHRER, Martin, BLUMENSTOCK, Gunnar, EHEHALT, Stefan, GOELZ, Rangmar, POETS, Christian, SCHÖNING, Martin

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The Effect of Vasospasm on Cerebral Perfusion: A Colour Duplex Study of the Extra- and Intracranial Cerebral Arteries von Schöning, Martin, Scheel, Peter, Wittibschläger, Jochen, Kehrer, Martin, Will, Bernd E

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12q24.33 deletion: Report of a patient with intellectual disability and review of the literature von Kehrer, Martin, Singer, Sylke, Grasshoff, Ute, Schäferhoff, Karin, Bonin, Michael, Riess, Olaf, Schöning, Martin, Tzschach, Andreas

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Einleitung von Kehrer, Martin

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Stimulation der menschlichen Sinne am Fahrsimulator von Kehrer, Martin

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Der Fahrsimulator von Kehrer, Martin

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