APA (7th ed.) Citation

Horn, D., Kapeller, J., Rivera-Brugués, N., Moog, U., Lorenz-Depiereux, B., Eck, S., . . . Strom, T. M. (2010). Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Human mutation, 31(11), . https://doi.org/10.1002/humu.21362

Chicago Style (17th ed.) Citation

Horn, Denise, et al. "Identification of FOXP1 Deletions in Three Unrelated Patients with Mental Retardation and Significant Speech and Language Deficits." Human Mutation 31, no. 11 (2010). https://doi.org/10.1002/humu.21362.

MLA (9th ed.) Citation

Horn, Denise, et al. "Identification of FOXP1 Deletions in Three Unrelated Patients with Mental Retardation and Significant Speech and Language Deficits." Human Mutation, vol. 31, no. 11, 2010, https://doi.org/10.1002/humu.21362.