APA (7th ed.) Citation

Paganini, I., Sestini, R., Capone, G., Putignano, A., Contini, E., Giotti, I., . . . Papi, L. (2017). A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency. Clinical Genetics, 92(6), 664. https://doi.org/10.1111/cge.13085

Chicago Style (17th ed.) Citation

Paganini, I., et al. "A Novel PAX1 Null Homozygous Mutation in Autosomal Recessive Otofaciocervical Syndrome Associated with Severe Combined Immunodeficiency." Clinical Genetics 92, no. 6 (2017): 664. https://doi.org/10.1111/cge.13085.

MLA (9th ed.) Citation

Paganini, I., et al. "A Novel PAX1 Null Homozygous Mutation in Autosomal Recessive Otofaciocervical Syndrome Associated with Severe Combined Immunodeficiency." Clinical Genetics, vol. 92, no. 6, 2017, p. 664, https://doi.org/10.1111/cge.13085.