APA (7th ed.) Citation

Vuillaume, M., Jeanne, M., Laumonnier, F., Toutain, A., Ung, D., Quinquis, D., . . . Deleuze, J. (2018). Whole genome sequencing identifies a de novo 2.1 Mb balanced paracentric inversion disrupting FOXP1 and leading to severe intellectual disability. Clinica Chimica Acta, 485, 218. https://doi.org/10.1016/j.cca.2018.06.048

Chicago Style (17th ed.) Citation

Vuillaume, M.-L, et al. "Whole Genome Sequencing Identifies a De Novo 2.1 Mb Balanced Paracentric Inversion Disrupting FOXP1 and Leading to Severe Intellectual Disability." Clinica Chimica Acta 485 (2018): 218. https://doi.org/10.1016/j.cca.2018.06.048.

MLA (9th ed.) Citation

Vuillaume, M.-L, et al. "Whole Genome Sequencing Identifies a De Novo 2.1 Mb Balanced Paracentric Inversion Disrupting FOXP1 and Leading to Severe Intellectual Disability." Clinica Chimica Acta, vol. 485, 2018, p. 218, https://doi.org/10.1016/j.cca.2018.06.048.