1. Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma. Issue 1 (December 2015) Authors: Grotta, Simona; D'Elia, Gemma; Scavelli, Rossana; Genovese, Silvia; Surace, Cecilia; Sirleto, Pietro; Cozza, Raffaele; Romanzo, Antonino; De Ioris, Maria; Valente, Paola; Tomaiuolo, Anna; Lepri, Francesca; Franchin, Tiziana; Ciocca, Laura; Russo, Serena; Locatelli, Franco; Angioni, Adriano Journal: BMC cancer Issue: Volume 15:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature review. Issue 1 (12th November 2020) Authors: Arghir, Aurora; Papuc, Sorina Mihaela; Tutulan‐Cunita, Andreea‐Cristina; Erbescu, Alina; Loddo, Sara; Genovese, Silvia; Ciocca, Laura; Goldoni, Marina; Piscopo, Carmelo; Bernardini, Laura; Novelli, Antonio; Budisteanu, Magdalena Journal: Clinical case reports Issue: Volume 9:Issue 1(2021) Page Start: 314 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Hypoplastic left heart syndrome and 21q22.3 deletion. (7th February 2015) Authors: Ciocca, Laura; Digilio, M. Cristina; Lombardo, Antonietta; D'Elia, Gemma; Baban, Anwar; Capolino, Rossella; Petrocchi, Stefano; Russo, Serena; Sirleto, Pietro; Roberti, M. Cristina; Marino, Bruno; Angioni, Adriano; Dallapiccola, Bruno Journal: American journal of medical genetics Issue: Volume 167:Number 3(2015:Mar.) Page Start: 579 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗