Ehret, Julia K <br/><br/>
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?  [electronic resource] 

 -  Molecular cytogenetics  2015 
 - 72 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1755-8166 
<br/><br/><label>Standard No.: </label>10.1186/s13039-015-0178-8  doi