TY - JOUR TI - 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? T2 - Molecular Cytogenetics VL - 8 IS - 1 AU - Ehret, Julia K. and Engels, Hartmut and Cremer, Kirsten and Becker, Jessica and Zimmermann, Johannes P. and Wohlleber, Eva and Grasshoff, Ute and Rossier, Eva and Bonin, Michael and Mangold, Elisabeth and Bevot, Andrea and Schön, Stefanie and Heilmann-Heimbach, Stefanie and Dennert, Nicola and Mathieu-Dramard, Michèle and Lacaze, Elodie and Plessis, Ghislaine and de Broca, Alain and Jedraszak, Guillaume and Röthlisberger, Benno and Miny, Peter and Filges, Isabel and Dufke, Andreas and Andrieux, Joris and Lee, Jennifer A. and Zink, Alexander M. PB - Springer Science and Business Media LLC PY - 2015 PY - 2015 LA - English SN - 1755-8166 UR - http://dx.doi.org/10.1186/s13039-015-0178-8 UR - https://katalog.ub.uni-leipzig.de/Record/ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTE4Ni9zMTMwMzktMDE1LTAxNzgtOA ER -