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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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- المؤلفون: Ehret, Julia K.1; Engels, Hartmut1 ; Cremer, Kirsten1; Becker, Jessica1,2; Zimmermann, Johannes P.1; Wohlleber, Eva1,3; Grasshoff, Ute4; Rossier, Eva4,5; Bonin, Michael4,6; Mangold, Elisabeth1; Bevot, Andrea7; Schön, Stefanie1,8; Heilmann-Heimbach, Stefanie1,2; Dennert, Nicola1; Mathieu-Dramard, Michèle9; Lacaze, Elodie10; Plessis, Ghislaine10; de Broca, Alain11; Jedraszak, Guillaume9; Röthlisberger, Benno12
- المصدر:
Molecular Cytogenetics (17558166). 9/29/2015, Vol. 8 Issue 1, p1-14. 14p.
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