APA

Reuter M. S., Riess A., Moog U., Briggs T. A., Chandler K. E., Rauch A., Stampfer M., Steindl K., Gläser D., Joset P., Krumbiegel M., Rabe H., Schulte-Mattler U., Bauer P., Beck-Wödl S., Kohlhase J., Reis A. & Zweier C. (20171101). FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. : Journal of medical genetics.

Chicago

Reuter Miriam S, Riess Angelika, Moog Ute, Briggs Tracy A, Chandler Kate E, Rauch Anita, Stampfer Miriam, Steindl Katharina, Gläser Dieter, Joset Pascal, Krumbiegel Mandy, Rabe Harald, Schulte-Mattler Uta, Bauer Peter, Beck-Wödl Stefanie, Kohlhase Jürgen, Reis André and Zweier Christiane. 20171101. FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. : Journal of medical genetics.

Harvard

Reuter M. S., Riess A., Moog U., Briggs T. A., Chandler K. E., Rauch A., Stampfer M., Steindl K., Gläser D., Joset P., Krumbiegel M., Rabe H., Schulte-Mattler U., Bauer P., Beck-Wödl S., Kohlhase J., Reis A. and Zweier C. (20171101). FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. : Journal of medical genetics.

MLA

Reuter Miriam S, Riess Angelika, Moog Ute, Briggs Tracy A, Chandler Kate E, Rauch Anita, Stampfer Miriam, Steindl Katharina, Gläser Dieter, Joset Pascal, Krumbiegel Mandy, Rabe Harald, Schulte-Mattler Uta, Bauer Peter, Beck-Wödl Stefanie, Kohlhase Jürgen, Reis André and Zweier Christiane. FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. : Journal of medical genetics. 20171101.