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?
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S. Heilmann-Heimbach | A. Dufke | M. Bonin | U. Grasshoff | K. Cremer | E. Wohlleber | A. Zink | H. Engels | J. Andrieux | Jennifer A. Lee | P. Miny | E. Mangold | J. Becker | G. Plessis | M. Mathieu-Dramard | A. Bevot | E. Rossier | I. Filges | B. Röthlisberger | G. Jedraszak | A. de Broca | E. Lacaze | Nicola Dennert | Julia K. Ehret | Johannes P. Zimmermann | Stefanie Schön