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1 Ergebnisse
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Microdeletions in 9q33.3-q34.11 in five patients with intel..:
Ehret, Julia K.
;
Engels, Hartmut
;
Cremer, Kirsten
...
Molecular Cytogenetics. 8 (2015) 1 - p. , 2015
Link:
https://doi.org/10.1186/s13039-015-0178-8
RT Journal T1
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?
UL https://suche.suub.uni-bremen.de/peid=cr-10.1186_s13039-015-0178-8&Exemplar=1&LAN=DE A1 Ehret, Julia K. A1 Engels, Hartmut A1 Cremer, Kirsten A1 Becker, Jessica A1 Zimmermann, Johannes P. A1 Wohlleber, Eva A1 Grasshoff, Ute A1 Rossier, Eva A1 Bonin, Michael A1 Mangold, Elisabeth A1 Bevot, Andrea A1 Schön, Stefanie A1 Heilmann-Heimbach, Stefanie A1 Dennert, Nicola A1 Mathieu-Dramard, Michèle A1 Lacaze, Elodie A1 Plessis, Ghislaine A1 de Broca, Alain A1 Jedraszak, Guillaume A1 Röthlisberger, Benno A1 Miny, Peter A1 Filges, Isabel A1 Dufke, Andreas A1 Andrieux, Joris A1 Lee, Jennifer A. A1 Zink, Alexander M. PB Springer Science and Business Media LLC YR 2015 SN 1755-8166 JF Molecular Cytogenetics VO 8 IS 1 LK http://dx.doi.org/https://doi.org/10.1186/s13039-015-0178-8 DO https://doi.org/10.1186/s13039-015-0178-8 SF ELIB - SuUB Bremen
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