APA Citatie

Elli, F. M., deSanctis, L., Maffini, M., Bordogna, P., Tessaris, D., Pirelli, A., . . . Mantovani, G. (2019). Association of GNAS imprinting defects and deletions of chromosome 2 in two patients: Clues explaining phenotypic heterogeneity in pseudohypoparathyroidism type 1B/iPPSD3. Clin Epigenetics.

Chicago Style citaat

Elli, F. M., L. deSanctis, M.A Maffini, P. Bordogna, D. Tessaris, A. Pirelli, M. Arosio, A. Linglart, en G. Mantovani. "Association of GNAS Imprinting Defects and Deletions of Chromosome 2 in Two Patients: Clues Explaining Phenotypic Heterogeneity in Pseudohypoparathyroidism Type 1B/iPPSD3." Clin Epigenetics 2019.

MLA citatie

Elli, F. M., et al. "Association of GNAS Imprinting Defects and Deletions of Chromosome 2 in Two Patients: Clues Explaining Phenotypic Heterogeneity in Pseudohypoparathyroidism Type 1B/iPPSD3." Clin Epigenetics 2019.