Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions News feed Embed this list Save this search Mark all Export Your filters: cql: author="BALIKOVA, I" or (type exact bookEditor and editor="BALIKOVA, I") Mark journalArticle Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders. C Zeitz, C Michiels, M Neuillé, C Friedburg, C Condroyer, F Boyard, A Antonio, N Bouzidi, D Milicevic, R Veaux, et al. (2019) Hum Mutat. Mark journalArticle A1 Subtelomeric imbalances in phenotypically normal individuals I BALIKOVA, Björn Menten (UGent) , T DE RAVEL, C LE CAIGNEC, B THIENPONT, M URBINA, M DOCO-FENZY, M DE RADEMAEKER, Geert Mortier (UGent) , F KOOY, et al. (2007) HUMAN MUTATION. 28(10). p.958-967 Mark journalArticle A1 Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports Björn Menten (UGent) , N MAAS, B THIENPONT, Karen Buysse (UGent) , Jo Vandesompele (UGent) , C MELOTTE, T DE RAVEL, S VAN VOOREN, I BALIKOVA, L BACKX, et al. (2006) JOURNAL OF MEDICAL GENETICS. 43(8).