Li, Hong <br/><br/>
Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.  [electronic resource] 

 -  Brain & development  Apr 2005 
 - 207-10 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0387-7604 
<br/><br/><label>Standard No.: </label>10.1016/j.braindev.2004.06.002  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Autistic Disorder--genetics<br/>Child<br/>Child, Preschool<br/>Chromatography, High Pressure Liquid<br/>Chromosomes, Human, Pair 7--genetics<br/>DNA Mutational Analysis<br/>DNA Primers<br/>Female<br/>Forkhead Transcription Factors<br/>Humans<br/>Japan<br/>Male<br/>Mutation<br/>Polymerase Chain Reaction<br/>Transcription Factors--genetics