Cita APA

Yigit, G., Brown, K. E., Kayserili, H., Pohl, E., Caliebe, A., Zahnleiter, D., . . . Wollnik, B. (2015). Mutations in CDK5RAP2 cause Seckel syndrome. Mol Genet Genomic Med.

Citación estilo Chicago

Yigit, Gökhan, et al. "Mutations in CDK5RAP2 Cause Seckel Syndrome." Mol Genet Genomic Med 2015.

Cita MLA

Yigit, Gökhan, et al. "Mutations in CDK5RAP2 Cause Seckel Syndrome." Mol Genet Genomic Med 2015.