Feenstra, I <br/><br/>
Cryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literature.  [electronic resource] 

 -  European journal of medical genetics   
 - 384-95 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Review 
<br/><br/><label>ISSN: </label>1769-7212 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2006.01.005  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adult<br/>Aneuploidy<br/>Child, Preschool<br/>Chromosomes, Human, Pair 21--genetics<br/>Chromosomes, Human, Pair 22--genetics<br/>Developmental Disabilities--genetics<br/>Face--abnormalities<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Intellectual Disability--genetics<br/>Male<br/>Translocation, Genetic