De Filippis, R <br/><br/>
Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamics.  [electronic resource] 

 -  Clinical genetics  Oct 2012 
 - 395-403 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2011.01810.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Blotting, Western<br/>Child<br/>Chromatin--metabolism<br/>Chromosomes, Human, Pair 15--genetics<br/>DNA Methylation--genetics<br/>Female<br/>Fluorescence Recovery After Photobleaching<br/>Forkhead Transcription Factors--genetics<br/>Genetic Diseases, Inborn--genetics<br/>Humans<br/>Karyotyping<br/>Microscopy, Fluorescence<br/>Nerve Tissue Proteins--genetics<br/>Phenotype<br/>Point Mutation--genetics<br/>Syndrome