Baumer, A <br/><br/>
Non-random asynchronous replication at 22q11.2 favours unequal meiotic crossovers leading to the human 22q11.2 deletion.  [electronic resource] 

 -  Journal of medical genetics  Jun 2004 
 - 413-20 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.2003.016352  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22--genetics<br/>Crossing Over, Genetic--genetics<br/>DNA Replication--genetics<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Male<br/>Meiosis--genetics<br/>Microsatellite Repeats<br/>Models, Genetic<br/>Pedigree