APA (7th ed.) Citation

Mitter, D., Pringsheim, M., Kaulisch, M., Plümacher, K. S., Schröder, S., Warthemann, R., . . . Brockmann, K. (2018). FOXG1 syndrome: Genotype–phenotype association in 83 patients with FOXG1 variants. Genetics in medicine, 20(1), . https://doi.org/10.1038/gim.2017.75

Chicago Style (17th ed.) Citation

Mitter, Diana, et al. "FOXG1 Syndrome: Genotype–phenotype Association in 83 Patients with FOXG1 Variants." Genetics in Medicine 20, no. 1 (2018). https://doi.org/10.1038/gim.2017.75.

MLA (9th ed.) Citation

Mitter, Diana, et al. "FOXG1 Syndrome: Genotype–phenotype Association in 83 Patients with FOXG1 Variants." Genetics in Medicine, vol. 20, no. 1, 2018, https://doi.org/10.1038/gim.2017.75.