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Page 1
Subcutaneous diffuse neurofibroma of the neck: a case report.
de Varebeke SJ, De Schepper A, Hauben E, Declau F, Van Marck E, Van de Heyning PH. de Varebeke SJ, et al. Among authors: declau f. J Laryngol Otol. 1996 Feb;110(2):182-4. doi: 10.1017/s0022215100133122. J Laryngol Otol. 1996. PMID: 8729511
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p.
Van Camp G, Coucke PJ, Kunst H, Schatteman I, Van Velzen D, Marres H, van Ewijk M, Declau F, Van Hauwe P, Meyers J, Kenyon J, Smith SD, Smith RJ, Djelantik B, Cremers CW, Van de Heyning PH, Willems PJ. Van Camp G, et al. Among authors: declau f. Genomics. 1997 Apr 1;41(1):70-4. doi: 10.1006/geno.1997.4624. Genomics. 1997. PMID: 9126484 Free article.
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.
Coucke PJ, Van Hauwe P, Kelley PM, Kunst H, Schatteman I, Van Velzen D, Meyers J, Ensink RJ, Verstreken M, Declau F, Marres H, Kastury K, Bhasin S, McGuirt WT, Smith RJ, Cremers CW, Van de Heyning P, Willems PJ, Smith SD, Van Camp G. Coucke PJ, et al. Among authors: declau f. Hum Mol Genet. 1999 Jul;8(7):1321-8. doi: 10.1093/hmg/8.7.1321. Hum Mol Genet. 1999. PMID: 10369879
Audiometric analysis of a Belgian family linked to the DFNA10 locus.
Verstreken M, Declau F, Schatteman I, Van Velzen D, Verhoeven K, Van Camp G, Willems PJ, Kuhweide EW, Verhaert E, D'Haese P, Wuyts FL, Van de Heyning PH. Verstreken M, et al. Among authors: declau f. Am J Otol. 2000 Sep;21(5):675-81. Am J Otol. 2000. PMID: 10993457
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36.
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 RJ, Van Camp G. Van Den Bogaert K, et al. Among authors: declau f. Am J Hum Genet. 2001 Feb;68(2):495-500. doi: 10.1086/318185. Epub 2001 Jan 16. Am J Hum Genet. 2001. PMID: 11170898 Free PMC article.
60 results