Paduano, F., Colao, E., Loddo, S., Orlando, V., Trapasso, F., Novelli, A., . . . Iuliano, R. (2020). 7q35 Microdeletion and 15q13.3 and Xp22.33 Microduplications in a Patient with Severe Myoclonic Epilepsy, Microcephaly, Dysmorphisms, Severe Psychomotor Delay and Intellectual Disability. Genes (Basel).

Paduano, Francesco, Emma Colao, Sara Loddo, Valeria Orlando, Francesco Trapasso, Antonio Novelli, Nicola Perrotti, και Rodolfo Iuliano. "7q35 Microdeletion and 15q13.3 and Xp22.33 Microduplications in a Patient With Severe Myoclonic Epilepsy, Microcephaly, Dysmorphisms, Severe Psychomotor Delay and Intellectual Disability." Genes (Basel) 2020.

Paduano, Francesco, et al. "7q35 Microdeletion and 15q13.3 and Xp22.33 Microduplications in a Patient With Severe Myoclonic Epilepsy, Microcephaly, Dysmorphisms, Severe Psychomotor Delay and Intellectual Disability." Genes (Basel) 2020.