Doornbos, Marianne <br/><br/>
Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances.  [electronic resource] 

 -  European journal of medical genetics   
 - 108-15 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2009.03.010  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Angelman Syndrome--genetics<br/>Child<br/>Child, Preschool<br/>Chromosome Breakage<br/>Chromosome Deletion<br/>Chromosome Disorders--genetics<br/>Chromosomes, Human, Pair 15<br/>Family Health<br/>Humans<br/>Male<br/>Mental Disorders--genetics<br/>Prader-Willi Syndrome--genetics<br/>Speech Disorders<br/>Syndrome