De Crescenzo, A., Coppola, F., Falco, P., Bernardo, I., Ausanio, G., Cerrato, F., . . . Riccio, A. (2011). A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith–Wiedemann syndrome. Elsevier.

De Crescenzo, Agostina, Filomena Coppola, Pietro Falco, Italo Bernardo, Gaetano Ausanio, Flavia Cerrato, Luigi Falco, och Andrea Riccio. A Novel Microdeletion in the IGF2/H19 Imprinting Centre Region Defines a Recurrent Mutation Mechanism in Familial Beckwith–Wiedemann Syndrome. Elsevier, 2011.

De Crescenzo, Agostina, et al. A Novel Microdeletion in the IGF2/H19 Imprinting Centre Region Defines a Recurrent Mutation Mechanism in Familial Beckwith–Wiedemann Syndrome. Elsevier, 2011.