APA (7th ed.) Citation

S, D., D, B., I, D. V., E, R., F, K., & M, M. (2019). Novel BRPF1 mutation in a boy with intellectual disability, coloboma, facial nerve palsy and hypoplasia of the corpus callosum. European journal of medical genetics, 62(8), 103691. https://doi.org/10.1016/j.ejmg.2019.103691

Chicago Style (17th ed.) Citation

S, Demeulenaere, Beysen D, De Veuster I, Reyniers E, Kooy F, and Meuwissen M. "Novel BRPF1 Mutation in a Boy with Intellectual Disability, Coloboma, Facial Nerve Palsy and Hypoplasia of the Corpus Callosum." European Journal of Medical Genetics 62, no. 8 (2019): 103691. https://doi.org/10.1016/j.ejmg.2019.103691.

MLA (9th ed.) Citation

S, Demeulenaere, et al. "Novel BRPF1 Mutation in a Boy with Intellectual Disability, Coloboma, Facial Nerve Palsy and Hypoplasia of the Corpus Callosum." European Journal of Medical Genetics, vol. 62, no. 8, 2019, p. 103691, https://doi.org/10.1016/j.ejmg.2019.103691.