Tug, E <br/><br/>
A Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome.  [electronic resource] 

 -  Genetic counseling (Geneva, Switzerland)  2011 
 - 11-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1015-8146 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Brain--abnormalities<br/>Child<br/>Child Behavior Disorders--diagnosis<br/>Chromosome Banding<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 17--genetics<br/>Comparative Genomic Hybridization<br/>Female<br/>Genetic Counseling<br/>Humans<br/>Intellectual Disability--diagnosis<br/>Magnetic Resonance Imaging<br/>Phenotype<br/>Self-Injurious Behavior--diagnosis<br/>Smith-Magenis Syndrome--diagnosis