Prevention of serious hearing impairment of deafness in the young child.

Por Cremers, C W, van Rijn, P M, Hageman, M J
Publicado em 1989

Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications.

Por Kumar, S, Deffenbacher, K, Marres, H A, Cremers, C W, Kimberling, W J
Publicado em 2000

Genetic heterogeneity of Usher syndrome type II in a Dutch population.

Por Pieke-Dahl, S, van Aarem, A, Dobin, A, Cremers, C W, Kimberling, W J
Publicado em 1996

Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q

Por Pieke-Dahl, S, Moller, C, Kelley, P, Astuto, L, Cremers, C, Gorin, M, Kimberling, W
Publicado em 2000

Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping.

Por Kumar, S., Kimberling, W. J., Connolly, C. J., Tinley, S., Marres, H. A., Cremers, C. W.
Publicado em 1994

A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3

Por Snoeckx, R, Kremer, H, Ensink, R, Flothmann, K, de Brouwer, A, Smith, R, Cremers, C, Van Camp, G
Publicado em 2004

A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)

Por van Wijk, E, Krieger, E, Kemperman, M, De Leenheer, E M R, Huygen, P, Cremers, C, Cremers, F, Kremer, H
Publicado em 2003

Genomic Structure and Identification of Novel Mutations in Usherin, the Gene Responsible for Usher Syndrome Type IIa

Por Weston, M. D., Eudy, J. D., Fujita, S., Yao, S.-F., Usami, S., Cremers, C., Greenburg, J., Ramesar, R., Martini, A., Moller, C., Smith, R. J., Sumegi, J., Kimberling, William J.
Publicado em 2000

A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22–24

Por Van Den Bogaert, K, De Leenheer, E M R, Chen, W, Lee, Y, Nurnberg, P, Pennings, R, Vanderstraeten, K, Thys, M, Cremers, C, Smith, R, Van Camp, G
Publicado em 2004

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

Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.

Por Weston, M. D., Kelley, P. M., Overbeck, L. D., Wagenaar, M., Orten, D. J., Hasson, T., Chen, Z. Y., Corey, D., Mooseker, M., Sumegi, J., Cremers, C., Moller, C., Jacobson, S. G., Gorin, M. B., Kimberling, W. J.
Publicado em 1996

Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)

Por Bach, I., Brunner, H. G., Beighton, P., Ruvalcaba, R. H. A., Reardon, W., Pembrey, M. E., van der Velde-Visser, S. D., Bruns, G. A. P., Cremers, C. W. R. J., Cremers, F. P. M., Ropers, H.-H.
Publicado em 1992

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

CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness

Por Astuto, L. M., Bork, J. M., Weston, M. D., Askew, J. W., Fields, R. R., Orten, D. J., Ohliger, S. J., Riazuddin, S., Morell, R. J., Khan, S., Riazuddin, S., Kremer, H., van Hauwe, P., Moller, C. G., Cremers, C. W. R. J., Ayuso, C., Heckenlively, J. R., Rohrschneider, K., Spandau, U., Greenberg, J., Ramesar, R., Reardon, W., Bitoun, P., Millan, J., Legge, R., Friedman, T. B., Kimberling, W. J.
Publicado em 2002

Contribution of the N‐acetyltransferase 2 polymorphism NAT2*6A to age‐related hearing impairment

Por Van Eyken, E, Van Camp, G, Fransen, E, Topsakal, V, Hendrickx, J J, Demeester, K, Van de Heyning, P, Mäki‐Torkko, E, Hannula, S, Sorri, M, Jensen, M, Parving, A, Bille, M, Baur, M, Pfister, M, Bonaconsa, A, Mazzoli, M, Orzan, E, Espeso, A, Stephens, D, Verbruggen, K, Huyghe, J, Dhooge, I, Huygen, P, Kremer, H, Cremers, C W R J, Kunst, S, Manninen, M, Pyykkö, I, Lacava, A, Steffens, M, Wienker, T F, Van Laer, L
Publicado em 2007