Willemsen, M. H., Fernandez, B. A., Bacino, C. A., Gerkes, E., de Brouwer, A. P. M., Pfundt, R., . . . Kleefstra, T. (2010). Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome. European Journal of Human Genetics, 18(4), 429. https://doi.org/10.1038/ejhg.2009.192
Chicago Style (17th ed.) CitationWillemsen, Marjolein H., et al. "Identification of ANKRD11 and ZNF778 as Candidate Genes for Autism and Variable Cognitive Impairment in the Novel 16q24.3 Microdeletion Syndrome." European Journal of Human Genetics 18, no. 4 (2010): 429. https://doi.org/10.1038/ejhg.2009.192.
MLA (9th ed.) CitationWillemsen, Marjolein H., et al. "Identification of ANKRD11 and ZNF778 as Candidate Genes for Autism and Variable Cognitive Impairment in the Novel 16q24.3 Microdeletion Syndrome." European Journal of Human Genetics, vol. 18, no. 4, 2010, p. 429, https://doi.org/10.1038/ejhg.2009.192.