Innella G.; Greco D.; Carli D.; Magini P.; Giorgio E.; Galesi O.; Ferrero G.B.; Romano C.; Brusco A.; Graziano C., Clinical spectrum and follow-up in six individuals with Lamb–Shaffer syndrome (SOX5), «AMERICAN JOURNAL OF MEDICAL GENETICS. PART A», 2021, 185, pp. 608 - 613 [Scientific article]
Innella G.; Miccoli S.; Colussi D.; Pradella L.M.; Amato L.B.; Zuntini R.; Salfi N.C.M.; Collina G.; Ferrara F.; Ricciardiello L.; Turchetti D., Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review, «PATHOLOGY RESEARCH AND PRACTICE», 2021, 218, Article number: 153339 , pp. 1 - 7 [Scientific article]
Innella G.; Bonora E.; Neri I.; Virdi A.; Guglielmo A.; Pradella L.M.; Ceccarelli C.; Amato L.B.; Lanzoni A.; Miccoli S.; Gasparre G.; Zuntini R.; Turchetti D., PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis, «FRONTIERS IN MEDICINE», 2021, 8, Article number: 688105 , pp. 1 - 11 [Scientific article]Open Access
Isidori F.; Bozzarelli I.; Ferrari S.; Godino L.; Innella G.; Turchetti D.; Bonora E., Rasal1 and ros1 gene variants in hereditary breast cancer, «CANCERS», 2020, 12, Article number: 2539 , pp. 1 - 19 [Scientific article]Open Access
Innella G.; Rossi C.; Romagnoli M.; Repaci A.; Bianchi D.; Cantarini M.E.; Martorana D.; Godino L.; Pession A.; Percesepe A.; Pagotto U.; Turchetti D., Results and clinical interpretation of germline RET analysis in a series of patients with medullary thyroid carcinoma: The challenge of the variants of uncertain significance, «CANCERS», 2020, 12, Article number: 3268 , pp. 1 - 12 [Scientific article]Open Access
