Béna, Frédérique <br/><br/>
A de novo 1.1-1.6 Mb subtelomeric deletion of chromosome 20q13.33 in a patient with learning difficulties but without obvious dysmorphic features.  [electronic resource] 

 -  American journal of medical genetics. Part A  Aug 2007 
 - 1894-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.31789  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 20<br/>Face--abnormalities<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Learning Disabilities--genetics<br/>Oligonucleotide Array Sequence Analysis<br/>Strabismus--diagnosis<br/>Telomere--genetics