de Vries, Bert B A <br/><br/>
No evidence for submicroscopic 22qter deletions in patients with features suggestive for Angelman syndrome.  [electronic resource] 

 -  American journal of medical genetics  Apr 2002 
 - 117-20 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.10318  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Angelman Syndrome--genetics<br/>Blotting, Southern<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22--genetics<br/>DNA--genetics<br/>Family Health<br/>Female<br/>Humans<br/>Infant<br/>Male<br/>Microsatellite Repeats<br/>Pedigree