Itsara, Andy <br/><br/>
Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing.  [electronic resource] 

 -  American journal of human genetics  Apr 2012 
 - 599-613 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.2012.02.013  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Chromosome Breakpoints<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 17--genetics<br/>Comparative Genomic Hybridization--methods<br/>DNA Copy Number Variations<br/>Haplotypes<br/>Homologous Recombination<br/>Humans<br/>Molecular Sequence Data<br/>Segmental Duplications, Genomic<br/>Sequence Analysis, DNA--methods<br/>Smith-Magenis Syndrome