Nuttle, Xander <br/><br/>
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility.  [electronic resource] 

 -  Nature  08 2016 
 - 205-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. 
<br/><br/><label>ISSN: </label>1476-4687 
<br/><br/><label>Standard No.: </label>10.1038/nature19075  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Autistic Disorder--genetics<br/>Chromosome Breakage<br/>Chromosomes, Human, Pair 16--genetics<br/>DNA Copy Number Variations--genetics<br/>Evolution, Molecular<br/>Gene Duplication<br/>Genetic Predisposition to Disease<br/>Homeostasis--genetics<br/>Humans<br/>Iron--metabolism<br/>Pan troglodytes--genetics<br/>Pongo--genetics<br/>Proteins--analysis<br/>Recombination, Genetic<br/>Species Specificity<br/>Time Factors