Pubblicazioni

Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion

2020 - EUROPEAN JOURNAL OF MEDICAL GENETICS
Pascolini, G.; Valiante, M.; Bottillo, I.; Laino, L.; Fleischer, N.; Ferraris, A.; Grammatico, P.

Helsmoortel-Van der Aa Syndrome as emerging clinical diagnosis in intellectually disabled children with autistic traits and ocular involvement

2018 - EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
Pascolini, Giulia; Agolini, Emanuele; Majore, Silvia; Novelli, Antonio; Grammatico, Paola; Digilio, Maria Cristina

© Università degli Studi di Roma "La Sapienza" - Piazzale Aldo Moro 5, 00185 Roma