000 01620 a2200493 4500
005 20250517054356.0
264 0 _c20150930
008 201509s 0 0 eng d
022 _a1755-8166
024 7 _a10.1186/s13039-015-0178-8
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aEhret, Julia K
245 0 0 _aMicrodeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?
_h[electronic resource]
260 _bMolecular cytogenetics
_c2015
300 _a72 p.
_bdigital
500 _aPublication Type: Journal Article
700 1 _aEngels, Hartmut
700 1 _aCremer, Kirsten
700 1 _aBecker, Jessica
700 1 _aZimmermann, Johannes P
700 1 _aWohlleber, Eva
700 1 _aGrasshoff, Ute
700 1 _aRossier, Eva
700 1 _aBonin, Michael
700 1 _aMangold, Elisabeth
700 1 _aBevot, Andrea
700 1 _aSchön, Stefanie
700 1 _aHeilmann-Heimbach, Stefanie
700 1 _aDennert, Nicola
700 1 _aMathieu-Dramard, Michèle
700 1 _aLacaze, Elodie
700 1 _aPlessis, Ghislaine
700 1 _ade Broca, Alain
700 1 _aJedraszak, Guillaume
700 1 _aRöthlisberger, Benno
700 1 _aMiny, Peter
700 1 _aFilges, Isabel
700 1 _aDufke, Andreas
700 1 _aAndrieux, Joris
700 1 _aLee, Jennifer A
700 1 _aZink, Alexander M
773 0 _tMolecular cytogenetics
_gvol. 8
_gp. 72
856 4 0 _uhttps://doi.org/10.1186/s13039-015-0178-8
_zAvailable from publisher's website
999 _c25309886
_d25309886