Sollis, E., Fröhlich, H., & Rappold, G. (2016). Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder. Human molecular genetics, 25(3), . https://doi.org/10.1093/hmg/ddv495
Chicago-Zitierstil (17. Ausg.)Sollis, Elliot, Henning Fröhlich, und Gudrun Rappold. "Identification and Functional Characterization of De Novo FOXP1 Variants Provides Novel Insights into the Etiology of Neurodevelopmental Disorder." Human Molecular Genetics 25, no. 3 (2016). https://doi.org/10.1093/hmg/ddv495.
MLA-Zitierstil (9. Ausg.)Sollis, Elliot, et al. "Identification and Functional Characterization of De Novo FOXP1 Variants Provides Novel Insights into the Etiology of Neurodevelopmental Disorder." Human Molecular Genetics, vol. 25, no. 3, 2016, https://doi.org/10.1093/hmg/ddv495.