APA (7th ed.) Citation

Maria Giovanna Paglietti, Claudio Cherchi, Federica Porcaro, Emanuele Agolini, Alessandra Schiavino, Francesca Petreschi, . . . Renato Cutrera. (2019). Two novel mutations in exon 3 of PHOX2B gene: Think about congenital central hypoventilation syndrome in patients with Hirschsprung disease. BMC.

Chicago Style (17th ed.) Citation

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

MLA (9th ed.) Citation

Maria Giovanna Paglietti, et al. Two Novel Mutations in Exon 3 of PHOX2B Gene: Think About Congenital Central Hypoventilation Syndrome in Patients with Hirschsprung Disease. BMC, 2019.