APA (7th ed.) Citation

Rodriguez, S., Hall, A. J., Granell, R., McLean, W. H. I., Irvine, A. D., Palmer, C. N. A., . . . Day, I. N. M. Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohort. Public Library of Science (PLoS).

Chicago Style (17th ed.) Citation

Rodriguez, Santiago, Amanda J. Hall, Raquel Granell, W H Irwin McLean, Alan D. Irvine, Colin N A. Palmer, George Davey Smith, John Henderson, and Ian N M. Day. Carrier Status for the Common R501X and 2282del4 Filaggrin Mutations Is Not Associated with Hearing Phenotypes in 5,377 Children from the ALSPAC Cohort. Public Library of Science (PLoS).

MLA (9th ed.) Citation

Rodriguez, Santiago, et al. Carrier Status for the Common R501X and 2282del4 Filaggrin Mutations Is Not Associated with Hearing Phenotypes in 5,377 Children from the ALSPAC Cohort. Public Library of Science (PLoS).