APA (7th ed.) Citation

Snijders Blok, L., Kleefstra, T., Venselaar, H., Maas, S., Kroes, H. Y., Lachmeijer, A. M., . . . Fisher, S. E. (2019). De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder. American journal of human genetics, 105(2), 403-412. https://doi.org/10.1016/j.ajhg.2019.06.007

Chicago Style (17th ed.) Citation

Snijders Blok, Lot, et al. "De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder." American Journal of Human Genetics 105, no. 2 (2019): 403-412. https://doi.org/10.1016/j.ajhg.2019.06.007.

MLA (9th ed.) Citation

Snijders Blok, Lot, et al. "De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder." American Journal of Human Genetics, vol. 105, no. 2, 2019, pp. 403-412, https://doi.org/10.1016/j.ajhg.2019.06.007.