APA-viite

Palotie, A., Almusa, H., Saarela, J., Porkka, K., Trotta, L., Lepisto, M., . . . Syrjänen, J. (2016). Enrichment of rare variants in population isolates: Single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland. European Journal of Human Genetics, 24(10), p. 1473.

Chicago-tyylinen lähdeviittaus

Palotie, Aarno, et al. "Enrichment of Rare Variants in Population Isolates: Single AICDA Mutation Responsible for Hyper-IgM Syndrome Type 2 in Finland." European Journal of Human Genetics 24, no. 10 (2016): 1473.

MLA-viite

Palotie, Aarno, et al. "Enrichment of Rare Variants in Population Isolates: Single AICDA Mutation Responsible for Hyper-IgM Syndrome Type 2 in Finland." European Journal of Human Genetics 24.10 (2016): 1473.

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