Cita APA (7a ed.)

Haraldsdottir, S., Rafnar, T., Frankel, W. L., Einarsdottir, S., Sigurdsson, A., Hampel, H., . . . Stefansson, K. (2017). Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2. Nature Portfolio.

Cita Chicago Style (17a ed.)

Haraldsdottir, Sigurdis, et al. Comprehensive Population-wide Analysis of Lynch Syndrome in Iceland Reveals Founder Mutations in MSH6 and PMS2. Nature Portfolio, 2017.

Cita MLA (8a ed.)

Haraldsdottir, Sigurdis, et al. Comprehensive Population-wide Analysis of Lynch Syndrome in Iceland Reveals Founder Mutations in MSH6 and PMS2. Nature Portfolio, 2017.