APA (7e ed.) Bronvermelding

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.

Chicago (17e ed.) Bronvermelding

Graham, U., M. Nesbit, F. Hannan, SA Howles, R. Thakker, en 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.

MLA (9e ed.) Bronvermelding

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.