Cetin, Zafer <br/><br/>
A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement.  [electronic resource] 

 -  Gene  Mar 2013 
 - 176-80 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.2012.12.013  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Child, Preschool<br/>Chromosome Aberrations<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 5--genetics<br/>Cytogenetic Analysis<br/>Developmental Disabilities--genetics<br/>Follow-Up Studies<br/>Gene Rearrangement<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Intellectual Disability--genetics<br/>Karyotyping<br/>Male<br/>Translocation, Genetic