Bartlett, Christopher W <br/><br/>
Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment.  [electronic resource] 

 -  Human heredity  2004 
 - 10-20 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0001-5652 
<br/><br/><label>Standard No.: </label>10.1159/000077385  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Autistic Disorder--genetics<br/>Canada<br/>Chromosomes, Human, Pair 13<br/>Chromosomes, Human, Pair 2<br/>Chromosomes, Human, Pair 7<br/>Communication Disorders--genetics<br/>Cystic Fibrosis Transmembrane Conductance Regulator--genetics<br/>Genetic Linkage<br/>Genetic Markers<br/>Genotype<br/>Humans<br/>Language Disorders--genetics<br/>Linkage Disequilibrium<br/>Lod Score<br/>Models, Genetic<br/>Phenotype<br/>Statistics as Topic--methods<br/>United States