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Results: 1-4 |
Results: 4

Authors: Ensink, RJH Huygen, PLM Snoeckx, RL Caethoven, G Van Camp, G Cremers, CWRJ
Citation: Rjh. Ensink et al., A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13, CLIN OTOLAR, 26(4), 2001, pp. 310-316

Authors: Van Laer, L Coucke, P Mueller, RF Caethoven, G Flothmann, K Prasad, SD Chamberlin, GP Houseman, M Taylor, GR Van de Heyning, CM Fransen, E Rowland, J Cucci, RA Smith, RJH Van Camp, G
Citation: L. Van Laer et al., A common founder for the 35deIG GJB2 gene mutation in connexin 26 hearing impairment, J MED GENET, 38(8), 2001, pp. 515-518

Authors: Van den Bogaert, K Govaerts, PJ Schatteman, I Brown, MR Caethoven, G Offeciers, FE Somers, T Declau, F Coucke, P Van de Heyning, P Smith, RJH Van Camp, G
Citation: K. Van Den Bogaert et al., A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36, AM J HU GEN, 68(2), 2001, pp. 495-500

Authors: Bovee, JVMG Cleton-Jansen, AM Wuyts, W Caethoven, G Taminiau, AHM Bakker, E Van Hul, W Cornelisse, CJ Hogendoorn, PCW
Citation: Jvmg. Bovee et al., EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas, AM J HU GEN, 65(3), 1999, pp. 689-698
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