Ehret, Julia Engels, Hartmut Cremer, Kirsten Becker, Jessica Zimmermann, Johannes Wohlleber, Eva Grasshoff, Ute Rossier, Eva Bonin, Michael Mangold, Elisabeth Bevot, Andrea SchÜn, Stefanie Heilmann-Heimbach, Stefanie Dennert, Nicola Mathieu-Dramard, Michèle Lacaze, Elodie Plessis, Ghislaine de Broca, Alain Jedraszak, Guillaume RÜthlisberger, Benno Miny, Peter Filges, Isabel Dufke, Andreas Andrieux, Joris Lee, Jennifer Zink, Alexander Additional file 1: Table S1. of Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene? Sequencing results of GARNL3 in 192 patients with ID/DD. Microdeletion 9q33.3-q34.11;Intellectual disability;STXBP1;Contiguous gene syndrome;Haploinsufficiency 2015-09-29
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