APA (7th ed.) Citation

SR, T., K, M., AM, K., A, G., IB, T., RB, F., . . . AO, W. (2006). The origin of EFNB1 mutations in craniofrontonasal syndrome: Frequent somatic mosaicism and explanation of the paucity of carrier males. American journal of human genetics, 78(6), 999. https://doi.org/10.1086/504440

Chicago Style (17th ed.) Citation

SR, Twigg, et al. "The Origin of EFNB1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males." American Journal of Human Genetics 78, no. 6 (2006): 999. https://doi.org/10.1086/504440.

MLA (9th ed.) Citation

SR, Twigg, et al. "The Origin of EFNB1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males." American Journal of Human Genetics, vol. 78, no. 6, 2006, p. 999, https://doi.org/10.1086/504440.