APA (7th ed.) Citation

R, P., C, B., & CP, B. (2016). Hartsfield syndrome associated with a novel heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis. American journal of medical genetics. Part A, 170(8), 2222. https://doi.org/10.1002/ajmg.a.37731

Chicago Style (17th ed.) Citation

R, Prasad, Brewer C, and Burren CP. "Hartsfield Syndrome Associated with a Novel Heterozygous Missense Mutation in FGFR1 and Incorporating Tumoral Calcinosis." American Journal of Medical Genetics. Part A 170, no. 8 (2016): 2222. https://doi.org/10.1002/ajmg.a.37731.

MLA (9th ed.) Citation

R, Prasad, et al. "Hartsfield Syndrome Associated with a Novel Heterozygous Missense Mutation in FGFR1 and Incorporating Tumoral Calcinosis." American Journal of Medical Genetics. Part A, vol. 170, no. 8, 2016, p. 2222, https://doi.org/10.1002/ajmg.a.37731.