Vulto-van Silfhout, A., de Vries, B., van Bon, B., Hoischen, A., Ruiterkamp-Versteeg, M., Gilissen, C., . . . de Brouwer, A. (2013). Mutations in MED12 Cause X-Linked Ohdo Syndrome. American journal of human genetics, 92(3), 401-406. https://doi.org/10.1016/j.ajhg.2013.01.007
Chicago Style (17th ed.) CitationVulto-van Silfhout, Anneke T, et al. "Mutations in MED12 Cause X-Linked Ohdo Syndrome." American Journal of Human Genetics 92, no. 3 (2013): 401-406. https://doi.org/10.1016/j.ajhg.2013.01.007.
MLA (9th ed.) CitationVulto-van Silfhout, Anneke T, et al. "Mutations in MED12 Cause X-Linked Ohdo Syndrome." American Journal of Human Genetics, vol. 92, no. 3, 2013, pp. 401-406, https://doi.org/10.1016/j.ajhg.2013.01.007.
Warning: These citations may not always be 100% accurate.