1. A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment. Issue 8 (1st August 2001) Authors: Van Laer, L; Coucke, P; Mueller, R F; Caethoven, G; Flothmann, K; Prasad, S D; Chamberlin, G P; Houseman, M; Taylor, G R; Van de Heyning, C M; Fransen, E; Rowland, J; Cucci, R A; Smith, R J H; Van Camp, G Journal: Journal of medical genetics Issue: Volume 38:Issue 8(2001) Page Start: 515 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3. Issue 1 (16th January 2004) Authors: Snoeckx, R L; Kremer, H; Ensink, R J H; Flothmann, K; de Brouwer, A; Smith, R J H; Cremers, C W R J; Van Camp, G Journal: Journal of medical genetics Issue: Volume 41:Issue 1(2004) Page Start: 11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗