The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant.

MLA

Koolen, David A., 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, May 2016, pp. 652–59. EBSCOhost, https://doi.org/10.1038/ejhg.2015.178.

APA

Koolen, D. A., Pfundt, R., Linda, K., Beunders, G., Veenstra-Knol, H. E., Conta, J. H., Fortuna, A. M., Gillessen-Kaesbach, G., Dugan, S., Halbach, S., Abdul-Rahman, O. A., Winesett, H. M., Chung, W. K., Dalton, M., Dimova, P. S., Mattina, T., Prescott, K., Zhang, H. Z., Saal, H. M., … de Vries, B. B. A. (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), 652–659. https://doi.org/10.1038/ejhg.2015.178

Chicago

Koolen, David A, Rolph Pfundt, Katrin Linda, Gea Beunders, Hermine E Veenstra-Knol, Jessie H Conta, Ana Maria Fortuna, et al. 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): 652–59. doi:10.1038/ejhg.2015.178.