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="Perazzolo, Camille" or (type any "bookEditor issueEditor" and editor="Perazzolo, Camille") Add to list Journal Article A1 open access Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly : high incidence of epilepsy Sarah Duerinckx, Julie Désir, Camille Perazzolo, Cindy Badoer, Valérie Jacquemin, Julie Soblet, Isabelle Maystadt, Yusuf Tunca, Bettina Blaumeiser, Berten Ceulemans, et al. (2021) MOLECULAR GENETICS & GENOMIC MEDICINE. 9(9). Add to list Journal Article A1 open access Severe congenital microcephaly with AP4M1 mutation, a case report Sarah Duerinckx, Helene Verhelst (UGent) , Camille Perazzolo, Philippe David, Laurence Desmyter, Isabelle Pirson and Marc Abramowicz (2017) BMC MEDICAL GENETICS. 18. Add to list Journal Article A1 A familial heterozygous null mutation of MET in autism spectrum disorder Nelle Lambert, Vanessa Wermenbol, Bruno Pichon, Sandra Acosta, Jelle van den Ameele (UGent) , Camille Perazzolo, Diana Messina, Maria-Franca Musumeci, Barbara Dessars, Anne De Leener, et al. (2014) AUTISM RESEARCH. 7(5). p.617-622 Add to list Journal Article A1 FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly Nicolas Simonis, Isabelle Migeotte, Nelle Lambert, Camille Perazzolo, Deepthi C de Silva, Boyan Dimitrov, Claudine Heinrichs, Sandra Janssens (UGent) , Bronwyn Kerr, Geert Mortier, et al. (2013) JOURNAL OF MEDICAL GENETICS. 50(9). p.585-592