Reuter, M. (2017). FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. Journal of medical genetics, 54, . doi:10.1136/jmedgenet-2016-104094

"FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum / Miriam S. Reuter, Angelika Riess, Ute Moog, Tracy A. Briggs, Kate E. Chandler, Anita Rauch, Miriam Stampfer, Katharina Steindl, Dieter Gläser, Pascal Joset, D.D.D. Study, Mandy Krumbiegel, Harald Rabe, Uta Schulte-Mattler, Peter Bauer, Stefanie Beck-Wödl, Jürgen Kohlhase, André Reis, Christiane Zweier" Journal of Medical Genetics .

Reuter, Miriam. "FOXP2 Variants in 14 Individuals With Developmental Speech and Language Disorders Broaden the Mutational and Clinical Spectrum." Journal of Medical Genetics 54 (2017).