Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Save this search Download search results Subscribe to news feed Your filters: cql: author="Ramos, FJ" or (type any "bookEditor journalEditor issueEditor" and editor="Ramos, FJ") Add to list Journal Article A1 A novel domain-specific mutation in a sclerosteosis patient suggests a role of LRP4 as an anchor for sclerostin in human bone Igor Fijalkowski (UGent) , E Geets, E Steenackers, V Van Hoof, FJ Ramos, G Mortier, AM Fortuna, W Van Hul and E Boudin (2016) JOURNAL OF BONE AND MINERAL RESEARCH. 31(4). p.874-881 Add to list Journal Article A1 Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation MA DEARDORFF, M KAUR, D YAEGER, A RAMPURIA, S KOROLEV, J PIE, C GIL-RODRIGUEZ, M ARNEDO, Bart Loeys (UGent) , AD KLINE, et al. (2007) AMERICAN JOURNAL OF HUMAN GENETICS. 80(3). p.485-494