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: affiliation exact GE18 cql: author exact 801000049870 Add to list Journal Article A1 Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients Kristien Hoornaert (UGent) , Inge Vereecke (UGent) , Chantal Dewinter (UGent) , Thomas Rosenberg, Frits A Beemer, Juliaan Leroy (UGent) , Laila Bendix, Erik Björck, Maryse Bonduelle, Odile Boute, et al. (2010) EUROPEAN JOURNAL OF HUMAN GENETICS. 18(8). p.872-880 Add to list Journal Article A1 A new type of autosomal recessive spondyloepiphyseal dysplasia tarda Juliaan Leroy (UGent) , Bart Leroy (UGent) , LV Emmery, Ludwine Messiaen and JW Spranger (2004) AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 125A(1). p.49-56 Add to list Journal Article A1 Imaging studies in the diagnostic workup of neonatal nasal obstruction. Bart Vanzieleghem (UGent) , Marc Lemmerling (UGent) , Hubert Vermeersch (UGent) , P GOVAERT, Ingeborg Dhooge (UGent) , Françoise Meire (UGent) , Geert Mortier (UGent) , Juliaan Leroy (UGent) and Marc Kunnen (2001) JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY. 25(4). p.540-549 Add to list Journal Article A1 Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation: A new example of the Chitty syndrome. SG VANDAELE, Rudy Van Coster (UGent) , Françoise Meire (UGent) , AM SMETS and Juliaan Leroy (UGent) (1996) AMERICAN JOURNAL OF MEDICAL GENETICS. 65(3). p.205-208 Add to list Journal Article A1 Osteoporosis-pseudoglioma syndrome Anne De Paepe (UGent) , Juliaan Leroy (UGent) , Lieve Nuytinck (UGent) , Françoise Meire (UGent) and Jan Capoen (1993) AMERICAN JOURNAL OF MEDICAL GENETICS. 45(1). p.30-37