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="Vrijens, K" or (type any "bookEditor issueEditor" and editor="Vrijens, K") Add to list Journal Article A1 Characterization of the murine Dfna5 promoter and regulatory regions K Vrijens, G Van Camp and Lut Van Laer (UGent) (2009) GENE. 432(1-2). p.82-90 Add to list Journal Article A1 Human hereditary hearing impairment: mouse models can help to solve the puzzle K Vrijens, Lut Van Laer (UGent) and G Van Camp (2008) HUMAN GENETICS. 124(4). p.325-348 Add to list Journal Article A1 Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome K Vrijens, S Thys, MT De Jeu, AA Postnov, M Pfister, L Cox, A Zwijsen, V Van Hoof, M Mueller, NM De Clerck, et al. (2006) NEUROBIOLOGY OF DISEASE. 24(1). p.28-40 Add to list Journal Article A1 Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells Lut Van Laer (UGent) , M Pfister, S Thys, K Vrijens, M Mueller, L Umans, L Serneels, L Van Nassauw, F Kooy, RJH Smith, et al. (2005) NEUROBIOLOGY OF DISEASE. 19(3). p.386-399 Add to list Journal Article A1 DFNA5: hearing impairment exon instead of hearing impairment gene? Lut Van Laer (UGent) , K Vrijens, S Thys, VFI Van Tendeloo, RJH Smith, DR Van Bockstaele, JP Timmermans and G Van Camp (2004) JOURNAL OF MEDICAL GENETICS. 41(6). p.401-406