Rauch, Anita <br/><br/>
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.  [electronic resource] 

 -  Lancet (London, England)  Nov 2012 
 - 1674-82 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1474-547X 
<br/><br/><label>Standard No.: </label>10.1016/S0140-6736(12)61480-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Case-Control Studies<br/>Child<br/>Exome--genetics<br/>Female<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Mutation--genetics