1. Clinical and molecular characterization of Rubinstein‐Taybi syndrome patients carrying distinct novel mutations of the EP300 gene. (17th February 2014) Authors: Negri, G.; Milani, D.; Colapietro, P.; Forzano, F.; Della Monica, M.; Rusconi, D.; Consonni, L.; Caffi, L. G.; Finelli, P.; Scarano, G.; Magnani, C.; Selicorni, A.; Spena, S.; Larizza, L.; Gervasini, C. Journal: Clinical genetics Issue: Volume 87:Number 2(2015:Feb.) Page Start: 148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical utility of a targeted panel sequencing for the diagnosis of chronic hereditary liver diseases in adult patients. (March 2023) Authors: Marini, I.; Ronzoni, L.; Pelusi, S.; Golfetto, F.S.; Lombardi, A.; Rondena, J.; Periti, G.; Bianco, C.; Passignani, G.; Castronovo, P.; D'Ambrosio, R.; Finelli, P.; Prati, D.; Valenti, L. Journal: Digestive and liver disease Issue: Volume 55(2023)Supplement 1 Page Start: S35 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Developmental disorders with intellectual disability driven by chromatin dysregulation: Clinical overlaps and molecular mechanisms. Issue 2 (21st May 2018) Authors: Larizza, L.; Finelli, P. Journal: Clinical genetics Issue: Volume 95:Issue 2(2019) Page Start: 231 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗