Genetic insights into familial tumors of the nervous systemMELEAN, German; SESTINI, Roberta; AMMANNATI, Franco et al.American journal of medical genetics. 2004, Vol 129C, Num 1, pp 74-84, issn 0148-7299, 11 p.Article

Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in italian melanoma families displaying pancreatic cancer and neuroblastomaGHIORZO, Paola; GARGIULO, Sara; GENSINI, Francesca et al.Human molecular genetics (Print). 2006, Vol 15, Num 18, pp 2682-2689, issn 0964-6906, 8 p.Article

High-Resolution Melting Analysis for Rapid Detection of KRAS, BRAF, and PIK3CA Gene Mutations in Colorectal CancerSIMI, Lisa; PRATESI, Nicola; VIGNOLI, Marina et al.American journal of clinical pathology. 2008, Vol 130, Num 2, pp 247-253, issn 0002-9173, 7 p.Article

Premature ovarian failure and fragile X premutation: a study on 45 womenBUSSANI, Cecilia; PAPI, Laura; SESTINI, Roberta et al.European journal of obstetrics, gynecology, and reproductive biology. 2004, Vol 112, Num 2, pp 189-191, issn 0301-2115, 3 p.Article

Triple synchronous cutaneous melanoma : A clinical, dermoscopic, and genetic case studyDE GIORGI, Vincenzo; SALVINI, Camilla; SESTINI, Serena et al.Dermatologic surgery. 2007, Vol 33, Num 4, pp 488-491, issn 1076-0512, 4 p.Article

Neurofibromatosis type 2 attributable to gonosomal mosaicism in a clinically normal mother, and identification of seven novel mutations in the NF2 geneSESTINI, Roberta; VIVARELLI, Rossella; BALESTRI, Paolo et al.Human genetics. 2000, Vol 107, Num 4, pp 366-371, issn 0340-6717Article

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutationBACCI, Costanza; SESTINI, Roberta; PROVENZANO, Aldesia et al.Neurogenetics (Oxford. Print). 2010, Vol 11, Num 1, pp 73-80, issn 1364-6745, 8 p.Article