UZH-Logo

Maintenance Infos

Browse by Creators - Zurich Open Repository and Archive

Navigate back| Up a level
Export as
Number of items: 4.

Bader, Ingrid; Decker, E; Mayr, J A; Lunzer, V; Koch, J; Boltshauser, E; Sperl, W; Pietsch, P; Ertl-Wagner, B; Bolz, H; Bergmann, C; Rittinger, O (2016). MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum. European Journal of Medical Genetics, 59(8):386-391.

Becker, Jutta; Semler, O; Gilissen, C; Li, Y; Bolz, H J; Giunta, C; Bergmann, C; Rohrbach, M; Koerber, F; Zimmermann, K; de Vries, P; Wirth, B; Schoenau, E; Wollnik, B; Veltman, J A; Hoischen, A; Netzer, C (2011). Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta. American Journal of Human Genetics, 88(3):362-371.

Bergmann, C; Akhmetshina, A; Dees, C; Palumbo, K; Zerr, P; Beyer, C; Zwerina, J; Distler, O; Schett, G; Distler, J H W (2011). Inhibition of glycogen synthase kinase 3β induces dermal fibrosis by activation of the canonical Wnt pathway. Annals of the Rheumatic Diseases, 70(12):2191-2198.

Bergmann, C; Fliegauf, M; Brüchle, N O; Frank, V; Olbrich, H; Kirschner, J; Schermer, B; Schmedding, I; Kispert, A; Kränzlin, B; Nürnberg, G; Becker, C; Grimm, T; Girschick, G; Lynch, S A; Kelehan, P; Senderek, J; Neuhaus, T J; Stallmach, T; Zentgraf, H; Nürnberg, P; Gretz, N; Lohaus, C; Lienkamp, S; Schäfer, T; Walz, G; Benzing, T; Zerres, K; Omran, H (2008). Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia. American Journal of Human Genetics, 82(4):959-70.

This list was generated on Sat Jul 22 19:50:34 2017 CEST.