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References

These sources were used to develop the Genetics Home Reference condition summary on Smith-Magenis syndrome.

Gene Review: Smith-Magenis Syndrome
Girirajan S, Elsas LJ 2nd, Devriendt K, Elsea SH. RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions. J Med Genet. 2005 Nov;42(11):820-8. Epub 2005 Mar 23. PubMed citation
Girirajan S, Vlangos CN, Szomju BB, Edelman E, Trevors CD, Dupuis L, Nezarati M, Bunyan DJ, Elsea SH. Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum. Genet Med. 2006 Jul;8(7):417-27. PubMed citation
Gropman AL, Duncan WC, Smith AC. Neurologic and developmental features of the Smith-Magenis syndrome (del 17p11.2). Pediatr Neurol. 2006 May;34(5):337-50. Review. PubMed citation
Martin SC, Wolters PL, Smith AC. Adaptive and maladaptive behavior in children with Smith-Magenis Syndrome. J Autism Dev Disord. 2006 May;36(4):541-52. PubMed citation
Shelley BP, Robertson MM. The neuropsychiatry and multisystem features of the Smith-Magenis syndrome: a review. J Neuropsychiatry Clin Neurosci. 2005 Winter;17(1):91-7. Review. PubMed citation
Smith AC, Dykens E, Greenberg F. Behavioral phenotype of Smith-Magenis syndrome (del 17p11.2). Am J Med Genet. 1998 Mar 28;81(2):179-85. Review. PubMed citation
Tomona N, Smith AC, Guadagnini JP, Hart TC. Craniofacial and dental phenotype of Smith-Magenis syndrome. Am J Med Genet A. 2006 Dec 1;140(23):2556-61. PubMed citation

Reviewed: February 2007

Published: November 20, 2009