Semen Analysis in the Usher Syndrome Type 2A von van Aarem, A., Wagenaar, M., Tonnaer, E., Pieke Dahl, S., Bisseling, J., Janssen, H., Bastiaans, B., Kimberling, W., Cremers, C.

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Hearing impairment in Usher's syndrome von Pennings, R J E, Wagenaar, M, van Aarem, A, Huygen, P L M, Kimberling, W J, Cremers, C W R J

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Genetic heterogeneity of Usher syndrome type II in a Dutch population von Pieke-Dahl, S, van Aarem, A, Dobin, A, Cremers, C W, Kimberling, W J

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The electrooculogram in heterozygote carriers of Usher syndrome, retinitis pigmentosa, neuronal ceroid lipofuscinosis, Senior syndrome and choroideremia von Pinckers, A., van Aarem, A., Brink, H.

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Clinical findings in obligate carriers of type I Usher syndrome von Wagenaar, M., ter Rahe, B., van Aarem, A., Huygen, P., Admiraal, R., Bleeker-Wagemakers, E., Pinckers, A., Kimberling, W., Cremers, C.

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Colour vision in retinitis pigmentosa. Influence of cystoid macular edema von Pinckers, A, van Aarem, A, Keunen, J E

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Pure tone hearing thresholds and speech recognition scores in Dutch patients carrying mutations in the USH2A gene von PENNINGS, Ronald J. E, HUYGEN, Patrick L. M, WESTON, Michael D, VAN AAREM, Annelies, WAGENAAR, Mariette, KIMBERLING, William J, CREMERS, Cor W. R. J

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Gene mapping of Usher syndrome type IIa : localization of the gene to a 2.1-cM segment on chromosome 1q41 von KIMBERLING, W. J, WESTON, M. D, TAMAYO, M. L, BERNAL, J, GREENBERG, J, AYUSO, C, MÖLLER, C, VAN AAREM, A, CREMERS, C. W. R. J, SUMEGI, J, ING, P. S, CONNOLLY, C, MARTINI, A, MILANI, M

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Recurrent therapy resistant mastoiditis by Mycobacterium cheilonae abscessus, a nontuberculous mycobacterium von van Aarem, Annelies, Muytjens, Harry L, Smits, M.M, Cremers, Cor W.R.J

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The Usher syndrome type 2A: clinical findings in obligate carriers von van Aarem, Annelies, Cremers, Cor W.R.J., Pinckers, Alfred J.L.G., Huygen, Patrick L.M., Hombergen, Godfried C.J.H., Kimberling, Bill J.

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Long-term follow-up of chronic maxillary sinusitis in children von Otten, Floris W.A., van Aarem, Annelies, Grote, Jan J.

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Evaluation of visual impairment in Usher syndrome 1b and Usher syndrome 2a von Pennings, Ronald J. E., Huygen, Patrick L. M., Orten, Dana J., Wagenaar, Mariette, Van Aarem, Annelies, Kremer, Hannie, Kimberling, William J., Cremers, Cor W. R. J., Deutman, August F.

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Ophthalmologic findings in Usher syndrome type 2A von Aarem, Annelies Van, Wagenaar, Mariette, Pinckers, Alfred J. L. G., Huygen, Patrick L. M., Bleeker-wagemakers, Elisabeth M., Kimberling, Bill J., Cremers, W. R. J.

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Gene mapping of Usher syndrome type IIa: Localization of the gene to a 2.1-cM segment on chromosome 1q41 von Kimberling, W J, Weston, MD, Moeller, C, Van Aarem, A, Cremers, CWRJ, Sumegi, J, Ing, P S, Connolly, C, Martini, A, Milani, M, Tamayo, M L, Bernal, J, Greenberg, J, Ayuso, C

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USH2A Mutation analysis in 70 Dutch families with Usher syndrome type II von Pennings, Ronald J.E., te Brinke, Heleen, Weston, Michael D., Claassen, Annemarie, Orten, Dana J., Weekamp, Henriëtte, van Aarem, Annelies, Huygen, Patrick L.M., Deutman, August F., Hoefsloot, Lies H., Cremers, Frans P.M., Cremers, Cor W.R.J., Kimberling, William J., Kremer, Hannie

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Mapping of the Choroideremia-like (CHML) Gene at 1q42-qter and Mutation Analysis in Patients with Usher Syndrome Type II von v. Bokhoven, Hans, v. Genderen, Carolien, Molloy, Catherine M., v.d. Pol, Dorien J.R., Cremers, Cor W.R.J., v. Aarem, Annelies, Schwartz, Marianne, Rosenberg, Thomas, v. Kessel, Ad H.M.Geurts, Ropers, Hans Hilfiger, Cremers, Frans P.M.

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Case report of a unilateral cervical chondrocutaneous branchial remnant von van Kalkeren, Tjouwke A., Frima-van Aarem, Annelies, Ahsmann, Els J.M., Mahieu, Hans F.

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Pure Tone Hearing Thresholds and Speech Recognition Scores in Dutch Patients Carrying Mutations in the USH2A Gene von Ronald J.E.Pennings, Patrick L.M.Huygen, Michael D.Weston, Annelies van Aarem, Mariette Wagenaar, William J.Kimberling, Cor W.R.J.Cremers

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Lipid Metabolism in Rhizostoma von van Aarem, Helga K., Vonk, H. J., Zandee, D. I.

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