Yakut, Sezin <br/><br/>
Exceptional complex chromosomal rearrangement and microdeletions at the 4q22.3q23 and 14q31.1q31.3 regions in a patient with azoospermia.  [electronic resource] 

 -  Gene  Jan 2013 
 - 157-60 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1879-0038 
<br/><br/><label>Standard No.: </label>10.1016/j.gene.2012.09.063  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormal Karyotype<br/>Adult<br/>Azoospermia--genetics<br/>Chromosome Aberrations<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 1<br/>Chromosomes, Human, Pair 10<br/>Chromosomes, Human, Pair 14<br/>Chromosomes, Human, Pair 4<br/>Chromosomes, Human, Y<br/>Comparative Genomic Hybridization<br/>Humans<br/>Male<br/>Translocation, Genetic