Authors: Van Camp, Guy Snoeckx, Rikkert L Hilgert, Nele Van den Ende, Jenneke Fukuoka, Hisakumi Wagatsuma, Michio Suzuki, Hiroaki Smets, R.M. Erica Vanhoenacker, Filip Declau, Frank Van De Heyning, Paul Usami, Shin-ichi

Citation: Van Camp, Guy et al., A New Autosomal Recessive Form of Stickler Syndrome Is Caused by a Mutation in the COL9A1 Gene, American journal of human genetics , 79(3), 2006, pp. 449-457

Authors: Snoeckx, Rikkert L. Hugen, Patrick L.M. Feldmann, Delphine Marlin, Sandrine Denoyelle, Françoise Waligora, Jaroslaw Mueller-Malesinska, Malgorzata Pollak, Agneszka Ploski, Rafal Murgia, Alessandra Orzan, Eva Castorina, Pierangela Ambrosetti, Umberto Nowakowska-Szyrwinska, Ewa Bal, Jerzy Wiszniewski, Wojiciech Janecke, Andreas R. Nekahm-Heis, Doris Seeman, Pavel Bendova, Olga Kenna, Margaret A. Frangulov, Anna Rehm, Heidi L. Tekin, Mustafa Incesulu, Armagan Dahl, Hans-Henrik M. du Sart, Desirèe Jenksins, Lucy Lucas, Deirdre Bitner-Glindzicz, Maria Avraham, Karen B. Brownstein, Zippora del Castillo, Ignacio Moreno, Felipe Blin, Nikolaus Pfister, Markus Sziklai, Istvan Toth, Timea Kelley, Philip M. Cohn, Edward S. Van Maldergem, Lionel Hilbert, Pascale Roux, Anne-Françoise Mondain, Michel Hoefsloot, Lies H. Cremers, Cor W.R.J. Löppönen, Tuija Löppönen, Heikki Parving, Agnete Gronskov, Karen Schrijver, Iris Roberson, Joseph Gualandi, Francesca Martini, Alessandro Lina-Granade, Geneviève Pallares-Ruiz, Nathalie Correia, Céu Fialho, Graça Cryns, Kim Hilgert, Nele Van de Heyning, Paul Nishimura, Carla J. Smith, Richard J.H. Van Camp, Guy

Citation: L. Snoeckx, Rikkert et al., GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study, American journal of human genetics , 77(6), 2005, pp. 945-957