A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype - Zweier, Christiane; Kraus, Cornelia; Brueton, Louise; Cole, Trevor; Degenhardt, Franziska; Engels, Hartmut; Gillessen-Kaesbach, Gabriele; Graul-Neumann, Luitgard; Horn, Denise; Hoyer, Juliane; Just, Walter; Rauch, Anita; et al. (Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2013)
Aus: Journal of Medical Genetics 50.12 (2013): S. 838-847. <http://jmg.bmj.com/content/50/12/838>