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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 19, 2006
The yield of subtelomeric FISH analysis in the evaluation of autistic spectrum disordersAgatino Battaglia, Maria C BonagliaJournal of Child Neurology|September 30, 2016
Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients With Agenesis of the Corpus CallosumRomina Romaniello, Susan Marelli, Roberto Giorda, et al.Human Mutation|May 12, 2009
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological functionChiara Vantaggiato, Francesca Redaelli, Sestina Falcone, et al.European Journal of Medical Genetics|April 29, 2023
Consensus recommendations on counselling in Phelan-McDermid syndrome, with special attention to recurrence risk and to ring chromosome 22Sylvia A Koza, Anne C Tabet, Maria C Bonaglia, et al.European Journal of Human Genetics : EJHG|July 22, 2010
Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletionsMaria C Bonaglia, Susan Marelli, Francesca Novara, et al.Seizure|April 8, 2021
Electroclinical features of MEF2C haploinsufficiency-related epilepsy: A multicenter European studyFederico Raviglione, Sofia Douzgou, Marcello Scala, et al.Pageof 1