MARIANI, MILENA
MARIANI, MILENA
Universita' degli Studi di MILANO
13q mosaic deletion including RB1 associated to mild phenotype and no cancer outcome-case report and review of the literature
2018 I. Bestetti, A. Sironi, I. Catusi, M. Mariani, D. Giardino, S. Manoukian, D. Milani, L. Larizza, C. Castronovo, P. Finelli
Broadening of cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotype
2016 I. Parenti, C. Gervasini, J. Pozojevic, L. Graul Neumann, J. Azzollini, D. Braunholz, E. Watrin, K.S. Wendt, A. Cereda, D. Cittaro, G. Gillessen Kaesbach, D. Lazarevic, M. Mariani, S. Russo, R. Werner, P. Krawitz, L. Larizza, A. Selicorni, F.J. Kaiser
Cervical spine malformation in Cornelia de Lange syndrome: a report of three patients
2014 L.R. Bettini, L. Locatelli, M. Mariani, P. Cianci, C. Giussani, F. Canonico, A. Cereda, S. Russo, C. Gervasini, A. Biondi, A. Selicorni
Chromatinopathies: a focus on Cornelia de Lange Syndrome
2020 L. Avagliano, I. Parenti, P. Grazioli, E. Di Fede, C. Parodi, M. Mariani, F.J. Kaiser, A. Selicorni, C. Gervasini, V. Massa
Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome
2017 L. Avagliano, P. Grazioli, M. Mariani, G.P. Bulfamante, S. Angelo, V. Massa
Use of nutritional devices in Cornelia de Lange syndrome: Data from a large Italian cohort
2018 V. Decimi, B. Parma, R. Panceri, C. Fossati, M. Mariani, S. Russo, C.C. Gervasini, M. Cheli, A. Cereda, A. Selicorni