Cita APA

Mio, C., Allegri, L., Passon, N., Bregant, E., Demori, E., Franzoni, A., . . . Baldan, F. (2020). A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype. Eur J Hum Genet.

Chicago Style Citation

Mio, Catia, et al. "A Paternally Inherited 1.4 kb Deletion of the 11p15.5 Imprinting Center 2 Is Associated With a Mild Familial Silver–Russell Syndrome Phenotype." Eur J Hum Genet 2020.

Cita MLA

Mio, Catia, et al. "A Paternally Inherited 1.4 kb Deletion of the 11p15.5 Imprinting Center 2 Is Associated With a Mild Familial Silver–Russell Syndrome Phenotype." Eur J Hum Genet 2020.