Kurahashi, H <br/><br/>
The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.  [electronic resource] 

 -  Clinical genetics  Oct 2010 
 - 299-309 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2010.01445.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>AT Rich Sequence<br/>Chromosome Aberrations<br/>Chromosome Breakpoints<br/>Chromosomes, Human, Pair 11<br/>Chromosomes, Human, Pair 22<br/>DNA, Cruciform<br/>DNA, Single-Stranded--genetics<br/>Female<br/>Genome, Human<br/>Genomic Instability<br/>Humans<br/>Male<br/>Repetitive Sequences, Nucleic Acid<br/>Spermatogenesis<br/>Translocation, Genetic