A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndrome
KALAY, E, DE BROUWER, A. P. M, BRUNNER, H. G, KREMER, H, CAYLAN, R, NABUURS, S. B, WOLLNIK, B, KARAGUZEL, A, HEISTER, J. G. A. M, ERDOL, H, CREMERS, F. P. M, CREMERS, C. W. R. J
Published in Journal of molecular medicine (Berlin, Germany) (01.12.2005)
Published in Journal of molecular medicine (Berlin, Germany) (01.12.2005)
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A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4
KALAY, E, CAYLAN, R, KREMER, H, KIROGLU, A. F, YASAR, T, COLLIN, R. W. J, HEISTER, J. G. A. M, OOSTRIK, J, CREMERS, C. W. R. J, BRUNNER, H. G, KARAGUZEL, A
Published in Journal of molecular medicine (Berlin, Germany) (01.04.2007)
Published in Journal of molecular medicine (Berlin, Germany) (01.04.2007)
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Ear and hearing problems in relation to karyotype in children with Turner syndrome
Verver, E.J.J., Freriks, K., Thomeer, H.G.X.M., Huygen, P.L.M., Pennings, R.J.E., Alfen-van der Velden, A.A.E.M., Timmers, H.J., Otten, B.J., Cremers, C.W.R.J., Kunst, H.P.M.
Published in Hearing research (01.05.2011)
Published in Hearing research (01.05.2011)
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Sound localization with bilateral bone conduction devices
Caspers, Coosje J. I., Janssen, A. M., Agterberg, M. J. H., Cremers, C. W. R. J., Hol, M. K. S., Bosman, A. J.
Published in European archives of oto-rhino-laryngology (01.04.2022)
Published in European archives of oto-rhino-laryngology (01.04.2022)
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A comparative study of voice complaints and risk factors for voice complaints in female student teachers and practicing teachers early in their career
THOMAS, G, KOOIJMAN, P. G. C, CREMERS, C. W. R. J, DE JONG, F. I. C. R. S
Published in European archives of oto-rhino-laryngology (01.04.2006)
Published in European archives of oto-rhino-laryngology (01.04.2006)
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Validation of sonotubometry in healthy adults
van der Avoort, S J C, Heerbeek, N van, Zielhuis, G A, Cremers, C W R J
Published in Journal of laryngology and otology (01.10.2006)
Published in Journal of laryngology and otology (01.10.2006)
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Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q
Pieke-Dahl, S, Möller, C G, Kelley, P M, Astuto, L M, Cremers, C W R J, Gorin, M B, Kimberling, W J
Published in Journal of medical genetics (01.04.2000)
Published in Journal of medical genetics (01.04.2000)
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Journal Article
CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness
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.
Published in American journal of human genetics (01.08.2002)
Published in American journal of human genetics (01.08.2002)
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Contribution of the N-acetyltransferase 2 polymorphism NAT26A to age-related hearing impairment
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
Published in Journal of medical genetics (01.09.2007)
Published in Journal of medical genetics (01.09.2007)
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A new locus for otosclerosis, OTSC10, maps to chromosome 1q41-44
Schrauwen, I, Weegerink, NJD, Fransen, E, Claes, C, Pennings, RJE, Cremers, CWRJ, Huygen, PLM, Kunst, HPM, Van Camp, G
Published in Clinical genetics (01.05.2011)
Published in Clinical genetics (01.05.2011)
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Clinical report on the L95P mutation in a Dutch family with paraganglioma
Cremers, C W R J, De Mönnink, J P, Arts, N, Joosten, F B M, Kremer, H, Hoefsloot, L
Published in Otology & neurotology (01.09.2002)
Published in Otology & neurotology (01.09.2002)
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Journal Article
Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1–2q23.3
van Beelen, E., Schraders, M., Huygen, P.L.M., Oostrik, J., Plantinga, R.F., van Drunen, W., Collin, R.W.J., Kooper, D.P., Pennings, R.J.E., Cremers, C.W.R.J., Kremer, H., Kunst, H.P.M.
Published in Hearing research (01.06.2013)
Published in Hearing research (01.06.2013)
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Journal Article
A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22–24
Van Den Bogaert, K, De Leenheer, E M R, Chen, W, Lee, Y, Nürnberg, P, Pennings, R J E, Vanderstraeten, K, Thys, M, Cremers, C W R J, Smith, R J H, Van Camp, G
Published in Journal of medical genetics (01.06.2004)
Published in Journal of medical genetics (01.06.2004)
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