Pubblicazioni

Genetic counselling and high-penetrance susceptibility gene analysis reveal the novel CDKN2A p.D84V (c.251A>T) mutation in melanoma-prone families from Italy

2017 - MELANOMA RESEARCH

Borroni, Riccardo G.; Manganoni, Ausilia M.; Grassi, Sara; Grasso, Maurizia; Diegoli, Marta; Giorgianni, Carmela; Favalli, Valentina; Pavoni, Laura; Cespa, Maddalena; Arbustini, Eloisa

Characterization of endocrine features and genotype-phenotypes correlations in blepharophimosis-ptosis-epicanthus inversus syndrome type 1

2016 - JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

Nuovo, S.; Passeri, M.; Di Benedetto, E.; Calanchini, M.; Meldolesi, I.; Di Giacomo, M. C.; Petruzzi, D.; Piemontese, M. R.; Zelante, L.; Sangiuolo, F.; Novelli, G.; Fabbri, A.; Brancati, F.

A molecular study of pediatric spindle and sclerosing rhabdomyosarcoma identification of novel and recurrent VGLL2-related fusions in infantile cases

2016 - THE AMERICAN JOURNAL OF SURGICAL PATHOLOGY

Alaggio, Rita; Zhang, Lei; Sung, Yun Shao; Huang, Shih Chiang; Chen, Chun Liang; Bisogno, Gianni; Zin, Angelica; Agaram, Narasimhan P.; Laquaglia, Michael P.; Wexler, Leonard H.; Antonescu, Cristina R.