A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndrome von 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

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A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26) von van Wijk, E, Krieger, E, Kemperman, M H, De Leenheer, E M R, Huygen, P L M, Cremers, C W R J, Cremers, F P M, Kremer, H

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Clinical Neuroembryology: Development and Developmental Disorders of the Human Central Nervous System von Donkelaar, Hans J, Hori, Akira, Lammens, Martin

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A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4 von 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

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Ear and hearing problems in relation to karyotype in children with Turner syndrome von 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.

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Temporal bone anomalies in the branchio-oto-renal syndrome: Detailed Computed tomographic and magnetic resonance imaging findings von CERUTI, S, STINCKENS, C, CREMERS, C. W. R. J, CASSELMAN, J. W

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Sound localization with bilateral bone conduction devices von Caspers, Coosje J. I., Janssen, A. M., Agterberg, M. J. H., Cremers, C. W. R. J., Hol, M. K. S., Bosman, A. J.

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

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Genetic Hearing Impairment: Its Clinical Presentations von Cremers, Smith

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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 von THOMAS, G, KOOIJMAN, P. G. C, CREMERS, C. W. R. J, DE JONG, F. I. C. R. S

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Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q von Pieke-Dahl, S, Möller, C G, Kelley, P M, Astuto, L M, Cremers, C W R J, Gorin, M B, Kimberling, W J

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The Baha Softband. A new treatment for young children with bilateral congenital aural atresia von Verhagen, C V M, Hol, M K S, Coppens-Schellekens, W, Snik, A F M, Cremers, C W R J

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Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1–2q23.3 von 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.

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Contribution of the N-acetyltransferase 2 polymorphism NAT26A to age-related hearing impairment von 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

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Validation of sonotubometry in healthy adults von van der Avoort, S J C, Heerbeek, N van, Zielhuis, G A, Cremers, C W R J

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A new locus for otosclerosis, OTSC10, maps to chromosome 1q41-44 von Schrauwen, I, Weegerink, NJD, Fransen, E, Claes, C, Pennings, RJE, Cremers, CWRJ, Huygen, PLM, Kunst, HPM, Van Camp, G

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

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Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1 : evidence for genetic heterogeneity von MARIMAN, E. C. M, VAN BEERSUM, S. E. C, CREMERS, C. W. R. J, STRUYCKEN, P. M, ROPERS, H. H

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Otological aspects and surgical outcome in a consanguineous family with a novel ANKH gene mutation von Thomeer, H.G.X.M, Morava, E, Verbist, B.M, Cremers, C.W.R.J

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Progressive fluctuant hearing loss, enlarged vestibular aqueduct, and cochlear hypoplasia in branchio-oto-renal syndrome von KEMPERMAN, M. H, STINCKENS, C, KUMAR, S, HUYGEN, P. L. M, JOOSTEN, F. B. M, CREMERS, C. W. R. J

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