Molecular cytogenetic characterization of an interstitial deletion of chromosome 21 (21q22.13q22.3) in a patient with dysmorphic features, intellectual disability and severe generalized epilepsyAngelo Valetto, Giuseppe Saggese, Grazia Taddeucci et al.|European Journal of Medical Genetics|2012Cited by 68
A 6.5 mb deletion at 3q24q25.2 narrows Wisconsin syndrome critical region to a 750 kb interval: A potential role for <i>MBNLI</i>Veronica Bertini, Angelo Valetto, Alice Bonuccelli et al.|American Journal of Medical Genetics Part A|2016Cited by 34
DSM-5 criteria for PTSD in parents of pediatric patients with epilepsy: What are the changes with respect to DSM-IV-TR?Claudia Carmassi, Liliana Dell’Osso, Martina Corsi et al.|Epilepsy & Behavior|2017Cited by 23
17q12 Microduplications: A challenge for cliniciansVeronica Bertini, Angelo Valetto, Alessandro Orsini et al.|American Journal of Medical Genetics Part A|2015Cited by 8
A Case of 22q11 Deletion Syndrome (22q11DS) with a Panayiotopoulos Epileptic Pattern: Are Additional Copy-Number Variations a Possible Second Hit in Modulating the 22q11DS Phenotype?Veronica Bertini, Alice Bonuccelli, Angelo Valetto et al.|Frontiers in Pediatrics|2017Cited by 4