HuGE Literature Finder
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FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. Journal of medical genetics 2016 Aug . 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, Zweier Christia |
A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering. Neurobiology of disease 2014 Sep 69 23-31. Han Tae-Un, Park John, Domingues Carlos F, Moretti-Ferreira Danilo, Paris Emily, Sainz Eduardo, Gutierrez Joanne, Drayna Denn |
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