Epidural analgesia in gastrointestinal surgery von Fotiadis, R. J., Badvie, S., Weston, M. D., Allen-Mersh, T. G.

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

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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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Mutation of a Gene Encoding a Protein with Extracellular Matrix Motifs in Usher Syndrome Type IIa von Eudy, James D., Weston, Michael D., Yao, SuFang, Hoover, Denise M., Rehm, Heidi L., Ma-Edmonds, Manling, Yan, Denise, Ahmad, Iqbal, Cheng, Jason J., Ayuso, Carmen, Cremers, Cor, Davenport, Sandra, Moller, Claes, Talmadge, Catherine B., Beisel, Kirk W., Tamayo, Marta, Morton, Cynthia C., Swaroop, Anand, Kimberling, William J., Sumegi, Janos

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Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations von USAMI, S.-I, ABE, S, WESTON, M. D, SHINKAWA, H, VAN CAMP, G, KIMBERLING, W. J

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Defective myosin VIIA gene responsible for Usher syndrome type 1B von WEIL, D, BLANCHARD, S, KELLEY, P. M, KIMBERLING, W. J, WAGENAAR, M, LEVI-ACOBAS, F, LARGET-PIET, D, MUNNICH, A, STEEL, K. P, BROWN, S. D. M, PETIT, C, KAPLAN, J, GUILFORD, P, GIBSON, F, WALSH, J, MBURU, P, VARELA, A, LEVILLIERS, J, WESTON, M. D

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Phase I study of percutaneous cryotherapy for colorectal liver metastasis von Huang, A., McCall, J. M., Weston, M. D., Mathur, P., Quinn, H., Henderson, D. C., Allen-Mersh, T. G.

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Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients von WESTON, M. D, KELLEY, P. M, CREMERS, C, MÖLLER, C, JACOBSON, S. G, GORIN, M. B, KIMBERLING, W. J, OVERBECK, L. D, WAGENAAR, M, ORTEN, D. J, HASSON, T, CHEN, Z.-Y, COREY, D, MOOSEKER, M, SUMEGI, J

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Isolation of a Gene Encoding a Novel Member of the Nuclear Receptor Superfamily from the Critical Region of Usher Syndrome Type IIa at 1q41 von Eudy, James D., Yao, SuFang, Weston, Michael D., Ma-Edmonds, Manling, Talmadge, Catherine B., Cheng, Jason J., Kimberling, William J., Sumegi, Janos

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Linkage of usher syndrome type I gene (USH1B) to the long arm of chromosome 11 von Kimberling, W.J., Möller, C.G., Davenport, S., Priluck, I.A., Beighton, P.H., Greenberg, J., Reardon, W., Weston, M.D., Kenyon, J.B., Grunkemeyer, J.A., Pieke Dahl, S., Overbeck, L.D., Blackwood, D.J., Brower, A.M., Hoover, D.M., Rowland, P., Smith, R.J.H.

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Mivacurium in the myasthenic patient von PATERSON, I.G., HOOD, J.R., RUSSELL, S.H., WESTON, M.D., HIRECH, N.P.

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Isolation of a Novel Human Homologue of the Gene Coding for Echinoderm Microtubule-Associated Protein (EMAP) from the Usher Syndrome Type 1a Locus at 14q32 von Eudy, James D., Ma-Edmonds, Manling, Yao, Sufang, Talmadge, Catherine B., Kelley, Philip M., Weston, Michael D., Kimberling, William J., Sumegi, Janos

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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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Genetic heterogeneity of Usher syndrome type II von Pieke Dahl, S, Kimberling, W J, Gorin, M B, Weston, M D, Furman, J M, Pikus, A, Möller, C

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A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation von Dreyer, Bo, Tranebjærg, Lisbeth, Brox, Vigdis, Rosenberg, Thomas, Möller, Claes, Beneyto, Magdalena, Weston, Michael D., Kimberling, William J., Nilssen, Øivind

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Identification of novel USH2A mutations: implications for the structure of USH2A protein von Dreyer, B, Tranebjaerg, L, Rosenberg, T, Weston, M D, Kimberling, W J, Nilssen, O

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The Genomic Structure of the Gene Defective in Usher Syndrome Type Ib (MYO7A) von Kelley, Philip M., Weston, Mike D., Chen, Zheng-Yi, Orten, Dana J., Hasson, Tama, Overbeck, Larry D., Pinnt, Jeff, Talmadge, Catherine B., Ing, Paul, Mooseker, Mark S., Corey, David, Sumegi, Janos, Kimberling, William J.

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Genetic Heterogeneity of Usher Syndrome: Analysis of 151 Families with Usher Type I von Astuto, Lisa M., Weston, Michael D., Carney, Carol A., Hoover, Denise M., Cremers, Cor W.R.J., Wagenaar, Mariette, Moller, Claes, Smith, Richard J.H., Pieke-Dahl, Sandra, Greenberg, Jacquie, Ramesar, Raj, Jacobson, Samuel G., Ayuso, Carmen, Heckenlively, John R., Tamayo, Marta, Gorin, Michael B., Reardon, Willie, Kimberling, William J.

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Dinucleotide repeat polymorphism for D1S70 (CRI-L461) on chromosome 1q41 von Weston, M.D., Kimberling, W.J.

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Three novel mutations and twelve polymorphisms identified in the USH2A gene in Israeli USH2 families von Adato, Avital, Weston, Michael D., Berry, Asher, Kimberling, William J., Bonne-Tamir, Atsheva

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