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.

Volltext

Hayek, Gödel, and the case for methodological dualism von van den Hauwe, Ludwig M.P.

Volltext

The Dfna2 Locus for Hearing Impairment: Two Genes Regulating K+ Ion Recycling in the Inner Ear von van Hauwe, P., Coucke, P., van Camp, G.

Volltext

Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome von Coucke, P J, Van Hauwe, P, Everett, L A, Demirhan, O, Kabakkaya, Y, Dietrich, N L, Smith, R J H, Coyle, E, Reardon, W, Trembath, R, Willems, P J, Green, E D, Van Camp, G

Volltext

Deafness linked to DFNA2: one locus but how many genes? von Camp, Guy Van, Hauwe, Peter Van, Coucke, Paul J, Declau, Frank, Kunst, Henricus, Ensink, Robbert J, Marres, Henri A, Cremers, Cor W.R.J, Djelantik, Bulantrisna, Smith, Shelley D, Kelley, Phil, Heyning, Paul H. Van de

Volltext

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment von Verhoeven, Kristien, Laer, Lut Van, Kirschhofer, Karin, Legan, P. Kevin, Hughes, David C, Schatteman, Isabelle, Verstreken, Margriet, Hauwe, Peter Van, Coucke, Paul, Chen, Achih, Smith, Richard J.H, Somers, Thomas, Offeciers, F. Erwin, Heyning, Paul Van de, Richardson, Guy P, Wachtler, Franz, Kimberling, William J, Willems, Patrick J, Govaerts, Paul J, Camp, Guy Van

Volltext

Rho GTPase Cdc42 is essential for human T-cell development von SMITS, Kaatje, IANNUCCI, Veronica, STOVE, Veronique, VAN HAUWE, Peter, NAESSENS, Evelien, MEUWISSEN, Pieter J, ARIËN, Kevin K, BENTAHIR, Mostafa, PLUM, Jean, VERHASSELT, Bruno

Volltext

Mutations in the KCNQ4 Gene Are Responsible for Autosomal Dominant Deafness in Four DFNA2 Families von Coucke, Paul J., Van Hauwe, Peter, Kelley, Philip M., Kunst, Henricus, Schatteman, Isabelle, Van Velzen, Désirée, Meyers, Johan, Ensink, Robbert J., Verstreken, Margriet, Declau, Frank, Marres, Henri, Kastury, Kumar, Bhasin, Shalender, McGuirt, Wyman T., Smith, Richard J. H., Cremers, Cor W.R.J., Van de Heyning, Paul, Willems, Patrick J., Smith, Shelley D., Van Camp, Guy

Volltext

RP4::Mu3A-mediated in vivo cloning and transfer of a chlorobiphenyl catabolic pathway von Springael, Dirk, van Thor, Jasper, Goorissen, Heleen, Ryngaert, Annemie, De Baere, Raymond, Van Hauwe, Peter, Commandeur, Laetitia C. M, Parsons, John R, De Wachter, Rupert, Mergeay, Max

Volltext

A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 region von ENSINK, R. J. H, HUYGEN, P. L. M, VAN HAUWE, P, COUCKE, P, CREMERS, C. W. R. J, VAN CAMP, G

Volltext

Two Frequent Missense Mutations in Pendred Syndrome von Van Hauwe, Peter, Everett, Lorraine A., Coucke, Paul, Scott, Daryl A., Kraft, Michelle L., Ris-Stalpers, Carrie, Bolder, Cuny, Otten, Barto, de Vijlder, Jan J.M., Dietrich, Nicole L., Ramesh, Arabandi, Srisailapathy, Srikumari C. R., Parving, Agnete, Cremers, Cor W. R. J., Willems, Patrick J., Smith, Richard J. H., Green, Eric D., Van Camp, Guy

Volltext

DFNA 2, 5, 8, 12 von Van Camp, G, Coucke, P J, Van Hauwe, P, Van Laer, L, Verhoeven, K, Wuyts, F, Smith, R J

Volltext

Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family von DE BROUWER, Arjan P. M, PENNINGS, Ronald J. E, KIMBERLING, William J, CREMERS, Frans P. M, CREMERS, Cor W. R. J, KREMER, Hannie, ROETERS, Marjolijn, VAN HAUWE, Peter, ASTUTO, Lisa M, HOEFSLOOT, Lies H, HUYGEN, Patrick L. M, VAN DEN HELM, Bellinda, DEUTMAN, August F, BORK, Julie M

Volltext

An interlaboratory comparison of ITS2-PCR for the identification of yeasts, using the ABI Prism 310 and CEQ8000 capillary electrophoresis systems von De Baere, Thierry, Van Keerberghen, Anne, Van Hauwe, Peter, De Beenhouwer, Hans, Boel, An, Verschraegen, Gerda, Claeys, Geert, Vaneechoutte, Mario

Volltext

Nonsyndromic Autosomal Dominant Progressive Sensorineural Hearing Loss: Audiologic Analysis of a Pedigree Linked to DFNA2 von Kunst, Henricus, Marres, Henri, Huygen, Patrick, Ensink, Robert, Van Camp, Guy, Van Hauwe, Peter, Coucke, Paul, Willems, Patrick, Cremers, Cor

Volltext

Complementary deoxyribonucleic acid cloning and characterization of a putative human axonemal dynein light chain gene von KASTURY, K, TAYLOR, W. E, SHEN, R, ARVER, S, GUTIERREZ, M, FISHER, C. E, COUCKE, P. J, VAN HAUWE, P, VAN CAMP, G, BHASIN, S

Volltext

The Gene for Pendred Syndrome Is Located between D7S501 and D7S692 in a 1.7-cM Region on Chromosome 7q von Coucke, Paul, Van Camp, Guy, Demirhan, Osman, Kabakkaya, Yilmaz, Balemans, Wendy, Van Hauwe, Peter, Van Agtmael, Tom, Smith, Richard J.H., Parving, Agnete, Bolder, Cuny H.H.M., Cremers, Cor W.R.J., Willems, Patrick J.

Volltext

Chromosomal Mapping of Two Members of the Human Dynein Gene Family to Chromosome Regions 7p15 and 11q13 near the Deafness Loci DFNA 5 and DFNA 11 von Kastury, Kumar, Taylor, Wayne E., Gutierrez, Matthew, Ramirez, Luz, Coucke, Paul J., Van Hauwe, Peter, Van Camp, Guy, Bhasin, Shalender

Volltext

Linkage Analysis of Progressive Hearing Loss in Five Extended Families Maps the DFNA2 Gene to a 1.25-Mb Region on Chromosome 1p von Van Camp, Guy, Coucke, Paul J., Kunst, Hendrik, Schatteman, Isabelle, Van Velzen, Désirée, Marres, Henri, van Ewijk, Marleen, Declau, Frank, Van Hauwe, Peter, Meyers, Johan, Kenyon, Judy, Smith, Shelley D., Smith, Richard J.H., Djelantik, Bulantrisna, Cremers, Cor W.R.J., Van de Heyning, Paul H., Willems, Patrick J.

Volltext

Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region von Van Hauwe, Peter, Coucke, Paul J., Ensink, Robbert J., Huygen, Patrick, Cremers, Cor W.R.J., Van Camp, Guy

Volltext