Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="McGuirt, WT*" or (type exact bookEditor and editor="McGuirt, WT*") Add to list Journal Article A2 The phenotype of DFNA13/COL11A2. Els De Leenheer (UGent) , WT MCGUIRT, HP KUNST, PL HUYGEN, RJ SMITH and CW CREMERS (2002) ADVANCES IN OTO-RHINO-LARYNGOLOGY. 61. p.85-91 Add to list Journal Article A1 Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13). EMR De Leenheer, H Kunst, WT McGuirt, SD Prasad, M Brown, P Huygen, R Smith and WRJ Cremers (2001) ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY. 127(1). p.13-17 Add to list Journal Article A1 Autosomal dominant nonsyndromic hearing impairment Lut Van Laer (UGent) , WT McGuirt, T Yang, RJH Smith and G Van Camp (1999) AMERICAN JOURNAL OF MEDICAL GENETICS. 89(3). p.167-174 Add to list Journal Article A1 Nonsyndromic hearing impairment is associated with a mutation in DFNA5 Lut Van Laer (UGent) , EH Huizing, M Verstreken, D van Zuijlen, JG Wauters, PJ Bossuyt, P Van de Heyning, WT McGuirt, RJH Smith, PJ Willems, et al. (1998) NATURE GENETICS. 20(2). p.194-197