APA-referens

Sirmaci, A., Spiliopoulos, M., Brancati, F., Powell, E., Duman, D., Abrams, A., . . . Tekin, M. (2011). Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia. Elsevier.

Chicago-stil citat

Sirmaci, Asli, et al. Mutations in ANKRD11 Cause KBG Syndrome, Characterized By Intellectual Disability, Skeletal Malformations, and Macrodontia. Elsevier, 2011.

MLA-referens

Sirmaci, Asli, et al. Mutations in ANKRD11 Cause KBG Syndrome, Characterized By Intellectual Disability, Skeletal Malformations, and Macrodontia. Elsevier, 2011.

Varning: dessa hänvisningar är inte alltid fullständigt riktiga.