ATRX mutation in two adult brothers with non-specific moderate intellectual disability identified by exome sequencing()

por Moncini, S., Bedeschi, M.F., Castronovo, P., Crippa, M., Calvello, M., Garghentino, R.R., Scuvera, G., Finelli, P., Venturin, M.
Publicado 2013

High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function

por Bestetti, I, Castronovo, C, Sironi, A, Caslini, C, Sala, C, Rossetti, R, Crippa, M, Ferrari, I, Pistocchi, A, Toniolo, D, Persani, L, Marozzi, A, Finelli, P
Publicado 2019

Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency

por Bestetti, I, Barbieri, C, Sironi, A, Specchia, V, Yatsenko, S A, De Donno, M D, Caslini, C, Gentilini, D, Crippa, M, Larizza, L, Marozzi, A, Rajkovic, A, Toniolo, D, Bozzetti, M P, Finelli, P
Publicado 2021