Talkowski, Michael E <br/><br/>
Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research.  [electronic resource] 

 -  American journal of human genetics  Apr 2011 
 - 469-81 p.  digital 
<br/><br/> Publication Type: Comparative Study; Evaluation Study; 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.2011.03.013  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Inversion<br/>Chromosomes, Human--genetics<br/>Computational Biology<br/>DNA Barcoding, Taxonomic<br/>DNA Breaks<br/>Female<br/>Gene Library<br/>Gene Rearrangement<br/>Genome, Human<br/>Genome-Wide Association Study<br/>Humans<br/>Interspersed Repetitive Sequences<br/>Karyotyping<br/>Male<br/>Oligonucleotide Array Sequence Analysis<br/>Sequence Analysis, DNA--methods<br/>Translocation, Genetic