Fridman, C <br/><br/>
Prader-Willi syndrome: genetic tests and clinical findings.  [electronic resource] 

 -  Genetic testing  2000 
 - 387-92 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1090-6576 
<br/><br/><label>Standard No.: </label>10.1089/109065700750065144  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>DNA Methylation<br/>Female<br/>Genotype<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant<br/>Lymphocytes<br/>Male<br/>Microsatellite Repeats--genetics<br/>Phenotype<br/>Prader-Willi Syndrome--diagnosis<br/>Sequence Deletion--genetics