1. Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype. Issue 4 (14th January 2021) Authors: Tedesco, Maria Giovanna; Lonardo, Fortunato; Ceccarini, Caterina; Cesarano, Carla; Digilio, Maria Cristina; Magliozzi, Monia; Rogaia, Daniela; Mencarelli, Amedea; Leoni, Chiara; Piscopo, Carmelo; Imperatore, Valentina; Falco, Maria Teresa; Fontana, Paolo; Nardone, Anna Maria; Novelli, Antonio; Tr... Journal: American journal of medical genetics Issue: Volume 185:Issue 4(2021) Page Start: 1204 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Positive predictive values and outcomes for uninformative cell‐free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study). (30th November 2022) Authors: Grati, Francesca Romana; Bestetti, Ilaria; De Siero, Daria; Malvestiti, Francesca; Villa, Nicoletta; Sala, Elena; Crosti, Francesca; Parisi, Valentina; Nardone, Anna Maria; Di Giacomo, Gianluca; Pettinari, Antonella; Tortora, Giada; Montaldi, Annamaria; Calò, Annapaola; Saccilotto, Donatella; Zan... Journal: Prenatal diagnosis Issue: Volume 42:Number 13(2022) Page Start: 1575 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗