Neurologic and Developmental Features of the Smith-Magenis Syndrome (del 17p11.2)
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health
Reference62 articles.
1. Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2);Greenberg;Am J Med Genet,1996
2. Interstitial deletion of (17)(p11.2p11.2) in nine patients;Smith;Am J Med Genet,1986
3. Molecular analysis of the Smith-Magenis syndrome;Greenberg;Am J Hum Genet,1991
4. RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patients;Seranski;Gene,2001
5. Molecular screening for Smith-Magenis syndrome among patients with mental retardation of unknown cause;Struthers;J Med Genet,2002
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