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-Zitierstil (17. Ausg.)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-Zitierstil (9. Ausg.)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.