Gimelli, Stefania <br/><br/>
Array-CGH analysis in a patient with WAGR syndrome and a reciprocal translocation t(2;11) inherited from the normal father with double translocation.  [electronic resource] 

 -  American journal of medical genetics. Part A  Aug 2010 
 - 2130-3 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.33517  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosomes, Human, Pair 11--genetics<br/>Chromosomes, Human, Pair 2--genetics<br/>Comparative Genomic Hybridization<br/>Fathers<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant, Newborn<br/>Male<br/>Oligonucleotide Array Sequence Analysis<br/>Translocation, Genetic--genetics<br/>WAGR Syndrome--genetics