Ballesta Martínez, M J <br/><br/>
[Review of 22 patients with 22q11.2 deletion syndrome: phenotype spectrum].  [electronic resource] 

 -  Anales de pediatria (Barcelona, Spain : 2003)  Oct 2008 
 - 304-10 p.  digital 
<br/><br/> Publication Type: English Abstract; Journal Article 
<br/><br/><label>ISSN: </label>1695-4033 
<br/><br/><label>Standard No.: </label>10.1157/13126553  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>DiGeorge Syndrome--diagnosis<br/>Female<br/>Humans<br/>Infant<br/>Male<br/>Phenotype<br/>Retrospective Studies<br/>Young Adult