Nilsson, Daniel <br/><br/>
Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation.  [electronic resource] 

 -  Human mutation  02 2017 
 - 180-192 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.23146  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Chromosome Breakage<br/>Chromosome Mapping<br/>Comparative Genomic Hybridization<br/>DNA Copy Number Variations<br/>Female<br/>Genetic Association Studies<br/>Genomics--methods<br/>Genotype<br/>Homologous Recombination<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Karyotype<br/>Male<br/>Phenotype<br/>Translocation, Genetic<br/>Whole Genome Sequencing