High Prevalence of Symptoms of Menière's Disease in three Families With a Mutation in the COCH Gene
Fransen, Erik, Verstreken, Margriet, Verhagen, Wim I. M., Wuyts, Floris L., Huygen, Patrick L.M., D'Haese, Patrick, Robertson, Nahid G., Morton, Cynthia C., McGuirt, Wyman T., Smith, Richard J. H., Declau, Frank, Van de Heyning, Paul H., Van Camp, Guy
Published in Human molecular genetics (01.08.1999)
Published in Human molecular genetics (01.08.1999)
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Nonsyndromic hearing impairment is associated with a mutation in DFNA5
Van Camp, Guy, Laer, Lut Van, Huizing, Egbert H, Verstreken, Margriet, Zuijlen, Diederick van, Wauters, Jan G, Bossuyt, Paul J, Van de Heyning, Paul, McGuirt, Wyman T, Smith, Richard J.H, Willems, Patrick J, Legan, P. Kevin, Richardson, Guy P
Published in Nature genetics (01.10.1998)
Published in Nature genetics (01.10.1998)
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Journal Article
Mutations in the KCNQ4 Gene Are Responsible for Autosomal Dominant Deafness in Four DFNA2 Families
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
Published in Human molecular genetics (01.07.1999)
Published in Human molecular genetics (01.07.1999)
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Journal Article
Temporal bone histopathology in connexin 26-related hearing loss
Jun, A I, McGuirt, W T, Hinojosa, R, Green, G E, Fischel-Ghodsian, N, Smith, R J
Published in The Laryngoscope (01.02.2000)
Published in The Laryngoscope (01.02.2000)
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Journal Article
Localization of a Gene for Otosclerosis to Chromosome 15q25–q26
Tomek, Michael S., Brown, Matthew R., Mani, Sabitha R., Ramesh, Arabandi, Srikumari Srisailapathy, C. R., Coucke, Paul, Zbar, Ross I. S., Bell, Adam M., McGuirt, Wyman T., Fukushima, Kunihiro, Willems, Patrick J., Van Camp, Guy, Smith, Richard J. H.
Published in Human molecular genetics (01.02.1998)
Published in Human molecular genetics (01.02.1998)
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Definitive radiotherapy for early glottic carcinoma: Prognostic factors and implications for treatment
Burke, Lisa S., Greven, Kathryn M., McGuirt, Wyman T., Case, Douglas, Hoen, Helena M., Raben, Milton
Published in International journal of radiation oncology, biology, physics (15.07.1997)
Published in International journal of radiation oncology, biology, physics (15.07.1997)
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A Gene for Fluctuating, Progressive Autosomal Dominant Nonsyndromic Hearing Loss, DFNA16, Maps to Chromosome 2q23-24.3
Fukushima, Kunihiro, Kasai, Norio, Ueki, Yasuyoshi, Nishizaki, Kazunori, Sugata, Kennichi, Hirakawa, Satoshi, Masuda, Akemi, Gunduz, Mehmet, Ninomiya, Yoshifumi, Masuda, Yu, Sato, Minako, McGuirt, Wyman T., Coucke, Paul, Van Camp, Guy, Smith, Richard J.H.
Published in American journal of human genetics (01.07.1999)
Published in American journal of human genetics (01.07.1999)
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Journal Article
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)
Smith, Richard J.H, McGuirt, Wyman T, Prasad, Sai D, Griffith, Andrew J, Kunst, Henricus P.M, Green, Glenn E, Shpargel, Karl B, Runge, Christina, Huybrechts, Christy, Mueller, Robert F, Lynch, Eric, King, Mary-Claire, Brunner, Han G, Cremers, Cor W.R.J, Takanosu, Masamine, Li, Shi-Wu, Arita, Machiko, Mayne, Richard, Prockop, Darwin J, Camp, Guy Van
Published in Nature genetics (01.12.1999)
Published in Nature genetics (01.12.1999)
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Journal Article
Definitive radiotherapy for early glottic carcinoma: Prognostic factors and implications for treatment
Burke, Lisa S., Greven, Kathryn M., McGuirt, Wyman T., Case, Douglas, Hoen, Helena M., Raben, Milton
Published in International journal of radiation oncology, biology, physics (01.04.1997)
Published in International journal of radiation oncology, biology, physics (01.04.1997)
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Journal Article
Conference Proceeding
A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation
FRANSEN, ERIK, VERSTREKEN, MARGRIET, BOM, STEVEN J H, LEMAIRE, FRANÇOIS, KEMPERMAN, MARTIJN H, DE KOK, YVETTE J M, WUYTS, FLORIS L, VERHAGEN, WIM I M, HUYGEN, PATRICK L M, MCGUIRT, WYMAN T, SMITH, RICHARD J H, VAN MALDERGEM, LIONEL, DECLAU, FRANK, CREMERS, COR W R J, VAN DE HEYNING, PAUL H, CREMERS, FRANS P M, VAN CAMP, GUY
Published in Journal of medical genetics (01.01.2001)
Published in Journal of medical genetics (01.01.2001)
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Autosomal Dominant Inherited Hearing Impairment Caused by a Missense Mutation in COL11A2 (DFNA13)
De Leenheer, Els M. R, Kunst, Henricus P. M, McGuirt, Wyman T, Prasad, Sai D, Brown, Matthew R, Huygen, Patrick L. M, Smith, Richard J. H, Cremers, Cor W. R. J
Published in Archives of otolaryngology--head & neck surgery (01.01.2001)
Published in Archives of otolaryngology--head & neck surgery (01.01.2001)
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Consumption of a high-galactose diet induces diabetic-like changes in the inner ear
Raynor, E, Robison, W G, Garrett, C G, McGuirt, W T, Pillsbury, H C, Prazma, J
Published in Otolaryngology-head and neck surgery (01.12.1995)
Published in Otolaryngology-head and neck surgery (01.12.1995)
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Characterisation of DRASIC in the mouse inner ear
Hildebrand, Michael S., de Silva, Michelle G., Klockars, Tuomas, Rose, Elizabeth, Price, Margaret, Smith, Richard J.H., McGuirt, Wyman T., Christopoulos, Helen, Petit, Christine, Dahl, Hans-Henrik M.
Published in Hearing research (01.04.2004)
Published in Hearing research (01.04.2004)
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Journal Article
Intraparotid facial nerve neurofibromas
McGuirt, Sr, W Frederick, Johnson, Paul E, McGuirt, Wyman T
Published in The Laryngoscope (01.01.2003)
Published in The Laryngoscope (01.01.2003)
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Journal Article
Autosomal dominant nonsyndromic hearing impairment
Van Laer, L, McGuirt, W T, Yang, T, Smith, R J, Van Camp, G
Published in American journal of medical genetics (24.09.1999)
Published in American journal of medical genetics (24.09.1999)
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