A Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome. [electronic resource]
Producer: 20110711Description: 11-9 p. digitalISSN:- 1015-8146
- Brain -- abnormalities
- Child
- Child Behavior Disorders -- diagnosis
- Chromosome Banding
- Chromosome Deletion
- Chromosomes, Human, Pair 17 -- genetics
- Comparative Genomic Hybridization
- Female
- Genetic Counseling
- Humans
- Intellectual Disability -- diagnosis
- Magnetic Resonance Imaging
- Phenotype
- Self-Injurious Behavior -- diagnosis
- Smith-Magenis Syndrome -- diagnosis
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Publication Type: Case Reports; Journal Article
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