Dental Phenotype in Jalili Syndrome Due to a c.1312 dupC Homozygous Mutation in the CNNM4 Gene

by Luder, Hans U., Gerth-Kahlert, Christina, Ostertag-Benzinger, Silke, Schorderet, Daniel F.
Published 2013

Optical Coherence Tomography and Magnetic Resonance Imaging in Multiple Sclerosis and Neuromyelitis Optica Spectrum Disorder

by Manogaran, Praveena, Hanson, James V. M., Olbert, Elisabeth D., Egger, Christine, Wicki, Carla, Gerth-Kahlert, Christina, Landau, Klara, Schippling, Sven
Published 2016

Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center

by Gerth-Kahlert, Christina, Williamson, Kathleen, Ansari, Morad, Rainger, Jacqueline K, Hingst, Volker, Zimmermann, Theodor, Tech, Stefani, Guthoff, Rudolf F, van Heyningen, Veronica, FitzPatrick, David R
Published 2013

Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies

by Tiwari, Amit, Bahr, Angela, Bähr, Luzy, Fleischhauer, Johannes, Zinkernagel, Martin S., Winkler, Niklas, Barthelmes, Daniel, Berger, Lieselotte, Gerth-Kahlert, Christina, Neidhardt, John, Berger, Wolfgang
Published 2016