Cortés M, Fanny <br/><br/>
[Clinical, genetic and molecular features in 45 patients with Prader-Willi syndrome].  [electronic resource] 

 -  Revista medica de Chile  Jan 2005 
 - 33-41 p.  digital 
<br/><br/> Publication Type: English Abstract; Journal Article 
<br/><br/><label>ISSN: </label>0034-9887 
<br/><br/><label>Standard No.: </label>10.4067/s0034-98872005000100005  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Chile<br/>Female<br/>Gene Deletion<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Methylation<br/>Phenotype<br/>Prader-Willi Syndrome--diagnosis<br/>Retrospective Studies