학술논문
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?
Document Type
Article
Author
Ehret, J.K.; Engels, H.; Cremer, K.; Becker, J.; Zimmermann, J.P.; Wohlleber, E.; Mangold, E.; Schön, S.; Heilmann-Heimbach, S.; Dennert, N.; Lee, J.A.; Zink, A.M.; Grasshoff, U.; Rossier, E.; Bonin, M.; Dufke, A.; Bevot, A.; Mathieu-Dramard, M.; Jedraszak, G.; Lacaze, E.; Plessis, G.; De Broca, A.; Röthlisberger, B.; Miny, P.; Filges, I.; Andrieux, J.
Source
In: Molecular Cytogenetics . (Molecular Cytogenetics, 29 September 2015, 8(1))
Subject
Language
English
ISSN
17558166