Paglietti, M. G., Cherchi, C., Porcaro, F., Agolini, E., Schiavino, A., Petreschi, F., . . . Cutrera, R. (2019). Two novel mutations in exon 3 of PHOX2B gene: Think about congenital central hypoventilation syndrome in patients with Hirschsprung disease. Ital J Pediatr.

Paglietti, Maria Giovanna, Claudio Cherchi, Federica Porcaro, Emanuele Agolini, Alessandra Schiavino, Francesca Petreschi, Antonio Novelli, và Renato Cutrera. "Two Novel Mutations in Exon 3 of PHOX2B Gene: Think About Congenital Central Hypoventilation Syndrome in Patients With Hirschsprung Disease." Ital J Pediatr 2019.

Paglietti, Maria Giovanna, et al. "Two Novel Mutations in Exon 3 of PHOX2B Gene: Think About Congenital Central Hypoventilation Syndrome in Patients With Hirschsprung Disease." Ital J Pediatr 2019.