Migliavacca, Eugenia <br/><br/>
A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology.  [electronic resource] 

 -  American journal of human genetics  May 2015 
 - 784-96 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2015.04.002  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Brain<br/>Child<br/>Child Development Disorders, Pervasive--genetics<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 16--genetics<br/>Ciliary Body--metabolism<br/>DNA Copy Number Variations--genetics<br/>Gene Expression Regulation<br/>Humans<br/>Mice<br/>Potassium Channels, Voltage-Gated--genetics<br/>Schizophrenia--genetics<br/>Transcriptome<br/>Zebrafish<br/>Zebrafish Proteins--genetics