APA (7th ed.) Citation

DA, K., R, P., K, L., G, B., HE, V., JH, C., . . . BB, d. V. (2016). The Koolen-de Vries syndrome: A phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant. European journal of human genetics : EJHG, 24(5), 652. https://doi.org/10.1038/ejhg.2015.178

Chicago Style (17th ed.) Citation

DA, Koolen, et al. "The Koolen-de Vries Syndrome: A Phenotypic Comparison of Patients with a 17q21.31 Microdeletion Versus a KANSL1 Sequence Variant." European Journal of Human Genetics : EJHG 24, no. 5 (2016): 652. https://doi.org/10.1038/ejhg.2015.178.

MLA (9th ed.) Citation

DA, Koolen, et al. "The Koolen-de Vries Syndrome: A Phenotypic Comparison of Patients with a 17q21.31 Microdeletion Versus a KANSL1 Sequence Variant." European Journal of Human Genetics : EJHG, vol. 24, no. 5, 2016, p. 652, https://doi.org/10.1038/ejhg.2015.178.