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="Bitner-Glindzicz, Maria" or (type exact bookEditor and editor="Bitner-Glindzicz, Maria") Add to list Journal Article A1 DNA diagnostics of hereditary hearing loss : a targeted resequencing approach combined with a mutation classification system Manou Sommen, Isabelle Schrauwen, Geert Vandeweyer, Nele Boeckx, Jason J Corneveaux, Jenneke van den Ende, An Boudewyns, Els De Leenheer (UGent) , Sandra Janssens (UGent) , Kathleen Claes (UGent) , et al. (2016) HUMAN MUTATION. 37(8). p.812-819 Add to list Journal Article A1 A sensitive and specific diagnostic test for hearing loss using a microdroplet PCR-based approach and next generation sequencing Isabelle Schrauwen, Manou Sommen, Jason J Corneveaux, Rebecca A Reiman, Nicole J Hackett, Charlotte Claes, Kathleen Claes (UGent) , Maria Bitner-Glindzicz, Paul Coucke (UGent) , Guy Van Camp, et al. (2013) AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 161A(1). p.145-152 Add to list Journal Article A1 open access Development of a genotyping microarray for Usher syndrome Frans PM Cremers, William J Kimberling, Maigi Külm, Arjan P de Brouwer, Erwin van Wijk, Heleen te Brinke, Cor WRJ Cremers, Lies H Hoefsloot, Sandro Banfi, Francesca Simonelli, et al. (2007) JOURNAL OF MEDICAL GENETICS. 44(2). p.153-160