RINALDI, BERARDO
RINALDI, BERARDO
Universita' degli Studi di MILANO
Family history is key to the interpretation of exome sequencing in the prenatal context: unexpected diagnosis of Basal Cell Nevus Syndrome
2022 B. Rinaldi, C. Cesaretti, S. Boito, R. Villa, S. Guerneri, I. Borzani, T. Rizzuti, D. Marchetti, G. Conte, C. Cinnante, F. Triulzi, N. Persico, M. Iascone, F. Natacci
Incidental finding of APC deletion in a child: double trouble or double chance? – a case report
2021 E. Rosina, B. Rinaldi, R. Silipigni, L. Bergamaschi, G. Gattuso, S. Signoroni, S. Guerneri, A. Carnevali, P.G. Marchisio, D. Milani
Ocular features in Williams-Beuren syndrome: a review of the literature
2023 M. Nassisi, C. Mainetti, A. Aretti, A. Sperti, V. Nicotra, B. Rinaldi, F. Natacci, M.F. Bedeschi, F. Viola
Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology
2022 G. Moresco, O. Rondinone, A. Mauri, J. Costanza, C. Santaniello, P. Colapietro, E. Micaglio, G. Marfia, C. Pesenti, F. Grilli, B. Rinaldi, E. Prada, G. Scuvera, R. Villa, M.F. Bedeschi, M.R. Miozzo, D. Milani, L. Fontana