A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus

Por Van Camp, G., Kunst, H., Flothmann, K., McGuirt, W., Wauters, J., Marres, H., Verstreken, M., Bespalova, I., Burmeister, M., Van de Heyning, P. H, Smith, R., Willems, P., Cremers, C., Lesperance, M.
Publicado em 1999

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

Por Verhoeven, K, Van Camp, G, Govaerts, P J, Balemans, W, Schatteman, I, Verstreken, M, Van Laer, L, Smith, R J, Brown, M R, Van de Heyning, P H, Somers, T, Offeciers, F E, Willems, P J
Publicado em 1997

A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation

Por FRANSEN, E., VERSTREKEN, M., BOM, S., LEMAIRE, F., KEMPERMAN, M., DE KOK, Y. J M, WUYTS, F., VERHAGEN, W., HUYGEN, P., MCGUIRT, W., SMITH, R., VAN MALDERGEM, L., DECLAU, F., CREMERS, C., VAN DE HEYNING, P. H, CREMERS, F., VAN CAMP, G.
Publicado em 2001