Cita APA (7a ed.)

Graham, U., Nesbit, M., Hannan, F., Howles, S., Thakker, R., & Hunter, S. (2013). Familial Hypocalciuric Hypercalcaemia Type 3 (FHH3) Identified in a Family in Northern Ireland Leading to Identification of a Causative Mutation in the Adaptor Protein 2 Sigma 1 (AP2S1) Gene.

Cita Chicago Style (17a ed.)

Graham, U., M. Nesbit, F. Hannan, SA Howles, R. Thakker, y S. Hunter. Familial Hypocalciuric Hypercalcaemia Type 3 (FHH3) Identified in a Family in Northern Ireland Leading to Identification of a Causative Mutation in the Adaptor Protein 2 Sigma 1 (AP2S1) Gene. 2013.

Cita MLA (9a ed.)

Graham, U., et al. Familial Hypocalciuric Hypercalcaemia Type 3 (FHH3) Identified in a Family in Northern Ireland Leading to Identification of a Causative Mutation in the Adaptor Protein 2 Sigma 1 (AP2S1) Gene. 2013.

Precaución: Estas citas no son 100% exactas.