1. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes. Issue 1 (December 2016) Authors: Russo, Silvia; Calzari, Luciano; Mussa, Alessandro; Mainini, Ester; Cassina, Matteo; Di Candia, Stefania; Clementi, Maurizio; Guzzetti, Sara; Tabano, Silvia; Miozzo, Monica; Sirchia, Silvia; Finelli, Palma; Prontera, Paolo; Maitz, Silvia; Sorge, Giovanni; Calcagno, Annalisa; Maghnie, Mohamad; Div... Journal: Clinical epigenetics Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes. Issue 1 (December 2016) Authors: Russo, Silvia; Calzari, Luciano; Mussa, Alessandro; Mainini, Ester; Cassina, Matteo; Di Candia, Stefania; Clementi, Maurizio; Guzzetti, Sara; Tabano, Silvia; Miozzo, Monica; Sirchia, Silvia; Finelli, Palma; Prontera, Paolo; Maitz, Silvia; Sorge, Giovanni; Calcagno, Annalisa; Maghnie, Mohamad; Div... Journal: Clinical epigenetics Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A new case of Smith‐Kingsmore syndrome with somatic MTOR pathogenic variant expands the phenotypic spectrum to lateralized overgrowth. Issue 5 (8th February 2021) Authors: Carli, Diana; Ferrero, Giovanni Battista; Fusillo, Anna; Coppo, Paola; La Selva, Roberta; Zinali, Federica; Cardaropoli, Simona; Ranieri, Carlotta; Iacoviello, Matteo; Resta, Nicoletta; Mussa, Alessandro Journal: Clinical genetics Issue: Volume 99:Issue 5(2021) Page Start: 719 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Central adrenal insufficiency in young adults with Prader‐Willi Syndrome. (11th May 2013) Authors: Grugni, Graziano; Beccaria, Luciano; Corrias, Andrea; Crinò, Antonino; Cappa, Marco; De Medici, Clotilde; Di Candia, Stefania; Gargantini, Luigi; Ragusa, Letizia; Salvatoni, Alessandro; Sartorio, Alessandro; Spera, Sabrina; Andrulli, Simeone; Chiumello, Giuseppe; Mussa, Alessandro Journal: Clinical endocrinology Issue: Volume 79:Number 3(2013:Sep.) Page Start: 371 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Chronic subdural hematoma: A previously unreported life‐threatening complication in adult with Sotos syndrome. Issue 12 (14th October 2020) Authors: Carli, Diana; Gazzin, Andrea; Bongioanni, Maria Roberta; Bergui, Mauro; Mussa, Alessandro; Ferrero, Giovanni Battista Journal: American journal of medical genetics Issue: Volume 182:Issue 12(2020) Page Start: 3052 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Clinical and molecular characterization of patients affected by Beckwith‐Wiedemann spectrum conceived through assisted reproduction techniques. Issue 4 (21st July 2022) Authors: Carli, Diana; Operti, Matteo; Russo, Silvia; Cocchi, Guido; Milani, Donatella; Leoni, Chiara; Prada, Elisabetta; Melis, Daniela; Falco, Mariateresa; Spina, Jennifer; Uliana, Vera; Sara, Osimani; Sirchia, Fabio; Tarani, Luigi; Macchiaiolo, Marina; Cerrato, Flavia; Sparago, Angela; Pignata, Laura; ... Journal: Clinical genetics Issue: Volume 102:Issue 4(2022) Page Start: 314 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Comment on "Prenatal diagnosis and prognosis in Noonan syndrome". (December 2013) Authors: Baldassarre, Giuseppina; Mussa, Alessandro; Silengo, Margherita; Ferrero, Giovanni Battista Journal: Prenatal diagnosis Issue: Volume 33:Number 13(2013:Dec.) Page Start: 1318 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Constitutional bone impairment in Noonan syndrome. Issue 3 (17th February 2017) Authors: Baldassarre, Giuseppina; Mussa, Alessandro; Carli, Diana; Molinatto, Cristina; Ferrero, Giovanni Battista Journal: American journal of medical genetics Issue: Volume 173:Issue 3(2017) Page Start: 692 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Constitutional bone impairment in Noonan syndrome. Issue 3 (March 2017) Authors: Baldassarre, Giuseppina; Mussa, Alessandro; Carli, Diana; Molinatto, Cristina; Ferrero, Giovanni Battista Journal: American journal of medical genetics Issue: Volume 173:Issue 3(2017) Page Start: 692 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Cover Image, Volume 173A, Number 7, July 2017. Issue 7 (July 2017) Authors: Kalish, Jennifer M.; Biesecker, Leslie G.; Brioude, Frederic; Deardorff, Matthew A.; Di Cesare‐Merlone, Alessandra; Druley, Todd; Ferrero, Giovanni B.; Lapunzina, Pablo; Larizza, Lidia; Maas, Saskia; Macchiaiolo, Marina; Maher, Eamonn R.; Maitz, Silvia; Martinez‐Agosto, Julian A.; Mussa, Alessand... Journal: American journal of medical genetics Issue: Volume 173:Issue 7(2017) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗