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Number of items: 10.

Gerth-Kahlert, Christina; Tiwari, Amit; Hauri-Hohl, Mathias M; Hanson, James V M; Bahr, Angela; Palmowski-Wolfe, Anja; Güngör, Tayfun; Berger, Wolfgang (2017). Unusual retinopathy in a child with severe combined immune deficiency. Ophthalmic Genetics:Epub ahead of print.

Gerth-Kahlert, Christina; Tiwari, Amit; Hanson, James V M; Batmanabane, Vaishnavi; Traboulsi, Elias; Pennesi, Mark E; Al-Qahtani, Abdullah A; Lam, Byron L; Heckenlively, John; Zweifel, Sandrine A; Vincent, Ajoy; Fierz, Fabienne; Barthelmes, Daniel; Branham, Kari; Khan, Naheed; Bahr, Angela; Baehr, Luzy; Magyar, István; Koller, Samuel; Azzarello-Burri, Silvia; Niedrist, Dunja; Heon, Elise; Berger, Wolfgang (2017). C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations. Investigative Ophthalmology & Visual Science [IOVS], 58(10):3840-3850.

Medeiros-Domingo, Argelia; Saguner, Ardan M; Magyar, István; Bahr, Angela; Akdis, Deniz; Brunckhorst, Corinna; Duru, Firat; Berger, Wolfgang (2016). Arrhythmogenic right ventricular cardiomyopathy: implications of next-generation sequencing in appropriate diagnosis. Europace:Epub ahead of print.

Vincent, Ajoy; Ng, Judith; Gerth-Kahlert, Christina; Tavares, Erika; Maynes, Jason T; Wright, Thomas; Tiwari, Amit; Tumber, Anupreet; Li, Shuning; Hanson, James V M; Bahr, Angela; MacDonald, Heather; Bähr, Luzy; Westall, Carol; Berger, Wolfgang; Cremers, Frans P M; den Hollander, Anneke I; Héon, Elise (2016). Biallelic mutations in CRB1 underlie autosomal recessive familial foveal retinoschisis. Investigative Ophthalmology & Visual Science [IOVS], 57:2637-2646.

Tiwari, Amit; Bahr, Angela; Bähr, Luzy; Fleischhauer, Johannes; Zinkernagel, Martin S; Winkler, Niklas; Barthelmes, Daniel; Berger, Lieselotte; Gerth-Kahlert, Christina; Neidhardt, John; Berger, Wolfgang (2016). Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies. Scientific Reports, 6:28755.

Wilson, Anthony B; Whittington, Camilla M; Bahr, Angela (2014). High intralocus variability and interlocus recombination promote immunological diversity in a minimal major histocompatibility system. BMC Evolutionary Biology, 14(273):online.

Bahr, Angela; Sommer, Stefan; Mattle, Beat; Wilson, Anthony B (2012). Mutual mate choice in the potbellied seahorse (Hippocampus abdominalis). Behavioral Ecology, 23(4):869-878.

Bahr, Angela; Wilson, Anthony B (2012). The evolution of MHC diversity: Evidence of intralocus gene conversion and recombination in a single-locus system. Gene, 497(1):52-57.

Bahr, Angela. MHIIb Gene Diversity and Sexual Selection in the Potbellied Seahorse (Hippocampus abdominalis). 2011, University of Zurich, Faculty of Science.

Bahr, Angela; Wilson, Anthony B (2011). The impact of sex-role reversal on the diversity of the major histocompatibility complex: Insights from the seahorse (Hippocampus abdominalis). BMC Evolutionary Biology, 11:121.

This list was generated on Fri Sep 22 05:09:32 2017 CEST.