Pubblicazioni

GLI1 inactivation is associated with developmental phenotypes overlapping with Ellis-van Creveld syndrome

2017 - HUMAN MOLECULAR GENETICS

Palencia-Campos, A.; Ullah, A.; Nevado, J.; Yildirim, R.; Unal, E.; Ciorraga, M.; Barruz, P.; Chico, L.; Piceci-Sparascio, F.; Guida, V.; De Luca, A.; Kayserili, H.; Ullah, I.; Burmeister, M.; Lapunzina, P.; Ahmad, W.; Morales, A. V.; Ruiz-Perez, V. L.

A novel MGC4607/CCM2 gene mutation associated with cerebral spinal and cutaneous cavernous angiomas

2015 - JOURNAL OF MOLECULAR NEUROSCIENCE

Cigoli, M. S.; De Benedetti, S.; Marocchi, A.; Bacigaluppi, S.; Primignani, P.; Gesu, G.; Citterio, A.; Tassi, L.; Mecarelli, O.; Pulitano, P.; Penco, S.