Calounova, Gabriela <br/><br/>
Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation.  [electronic resource] 

 -  Neuro endocrinology letters  Oct 2006 
 - 579-85 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0172-780X 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Chromosomes, Human, Pair 15<br/>Chromosomes, Human, Pair 8<br/>Cytogenetic Analysis<br/>DNA Methylation<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Microsatellite Repeats<br/>Prader-Willi Syndrome--genetics<br/>Translocation, Genetic<br/>Uniparental Disomy--genetics