APA (7th ed.) Citation

M, J., RF, K., TJ, S., E, R., S, G., & F, T. (2018). A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome. European journal of medical genetics, 61(4), 209. https://doi.org/10.1016/j.ejmg.2017.11.016

Chicago Style (17th ed.) Citation

M, Jensen, Kooy RF, Simon TJ, Reyniers E, Girirajan S, and Tassone F. "A Higher Rare CNV Burden in the Genetic Background Potentially Contributes to Intellectual Disability Phenotypes in 22q11.2 Deletion Syndrome." European Journal of Medical Genetics 61, no. 4 (2018): 209. https://doi.org/10.1016/j.ejmg.2017.11.016.

MLA (9th ed.) Citation

M, Jensen, et al. "A Higher Rare CNV Burden in the Genetic Background Potentially Contributes to Intellectual Disability Phenotypes in 22q11.2 Deletion Syndrome." European Journal of Medical Genetics, vol. 61, no. 4, 2018, p. 209, https://doi.org/10.1016/j.ejmg.2017.11.016.