APA (7th ed.) Citation

J, O., CC, B., SB, D., JE, U., MJ, B., SS, B., . . . MJ, D. (2011). Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome. American journal of human genetics, 88(5), 616. https://doi.org/10.1016/j.ajhg.2011.04.005

Chicago Style (17th ed.) Citation

J, O'Sullivan, et al. "Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome." American Journal of Human Genetics 88, no. 5 (2011): 616. https://doi.org/10.1016/j.ajhg.2011.04.005.

MLA (9th ed.) Citation

J, O'Sullivan, et al. "Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome." American Journal of Human Genetics, vol. 88, no. 5, 2011, p. 616, https://doi.org/10.1016/j.ajhg.2011.04.005.