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Results: 1-6 |
Results: 6

Authors: Di Palma, F Holme, RH Bryda, EC Belyantseva, IA Pellegrino, R Kachar, B Steel, KP Noben-Trauth, K
Citation: F. Di Palma et al., Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D, NAT GENET, 27(1), 2001, pp. 103-107

Authors: Bolz, H von Brederlow, B Ramirez, A Bryda, EC Kutsche, K Nothwang, HG Seeliger, M Cabrera, MDS Vila, MC Molina, OP Gal, A Kubisch, C
Citation: H. Bolz et al., Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D, NAT GENET, 27(1), 2001, pp. 108-112

Authors: Bryda, EC Kim, HJ Legare, ME Frankel, WN Noben-Trauth, K
Citation: Ec. Bryda et al., High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and waltzer (Cdh23(v)), GENOMICS, 73(3), 2001, pp. 338-342

Authors: Bryda, EC Noben-Trauth, K Bureau, JF
Citation: Ec. Bryda et al., Mouse chromosome 10, MAMM GENOME, 11(11), 2000, pp. 951-952

Authors: Herron, BJ Bryda, EC Heverly, SA Collins, DN Flaherty, L
Citation: Bj. Herron et al., Scraggly, a new hair loss mutation on mouse Chromosome 19, MAMM GENOME, 10(9), 1999, pp. 864-869

Authors: Burmeister, M Bryda, EC Bureau, JF Noben-Trauth, K
Citation: M. Burmeister et al., Mouse Chromosome 10, MAMM GENOME, 10(10), 1999, pp. 950-951
Risultati: 1-6 |