Liégeois, F <br/><br/>
Endophenotypes of FOXP2: dysfunction within the human articulatory network.  [electronic resource] 

 -  European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society  Jul 2011 
 - 283-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1532-2130 
<br/><br/><label>Standard No.: </label>10.1016/j.ejpn.2011.04.006  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Basal Ganglia--physiopathology<br/>Brain--physiopathology<br/>Cerebellar Diseases--genetics<br/>Female<br/>Forkhead Transcription Factors--deficiency<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>Language Development Disorders--diagnosis<br/>Male<br/>Motor Cortex--physiopathology<br/>Nerve Net--physiopathology<br/>Phenotype<br/>Severity of Illness Index<br/>Speech--physiology