AAAAAA

   
Results: 1-2 |
Results: 2

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: Oldenburg, J von Brederlow, B Fregin, A Rost, S Wolz, W Eberl, W Eber, S Lenz, E Schwabb, R Brackmann, HH Effenberger, W Harbrecht, U Schurgers, LJ Vermeer, C Muller, CR
Citation: J. Oldenburg et al., Congenital deficiency of vitamin K dependent coagulation factors in two families presents as a genetic defect of the vitamin K-epoxide-reductase-complex, THROMB HAEM, 84(6), 2000, pp. 937-941
Risultati: 1-2 |