Reuter, M., & Moog, U. (2017). FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. Journal of medical genetics, 54(1), . https://doi.org/10.1136/jmedgenet-2016-104094
Chicago Style (17th ed.) CitationReuter, Miriam, and Ute Moog. "FOXP2 Variants in 14 Individuals with Developmental Speech and Language Disorders Broaden the Mutational and Clinical Spectrum." Journal of Medical Genetics 54, no. 1 (2017). https://doi.org/10.1136/jmedgenet-2016-104094.
MLA (9th ed.) CitationReuter, Miriam, and Ute Moog. "FOXP2 Variants in 14 Individuals with Developmental Speech and Language Disorders Broaden the Mutational and Clinical Spectrum." Journal of Medical Genetics, vol. 54, no. 1, 2017, https://doi.org/10.1136/jmedgenet-2016-104094.