Citação norma APA

Hempel, A., Pagnamenta, A. T., Blyth, M., Mansour, S., McConnell, V., Kou, I., . . . McNeill, A. (2016). Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome. J Med Genet.

Citação norma Chicago

Hempel, Annmarie, et al. "Deletions and De Novo Mutations of SOX11 Are Associated With a Neurodevelopmental Disorder With Features of Coffin–Siris Syndrome." J Med Genet 2016.

Citação norma MLA

Hempel, Annmarie, et al. "Deletions and De Novo Mutations of SOX11 Are Associated With a Neurodevelopmental Disorder With Features of Coffin–Siris Syndrome." J Med Genet 2016.

Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.