New developments in Smith-Magenis syndrome (del 17p11.2)
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Clinical Neurology,Neurology
Reference63 articles.
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2. Interstitial deletion of (17) (p11.2p11.2) in nine patients;Smith;Am J Med Genet,1986
3. RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patients;Seranski;Gene,2001
4. Mutations in RAI1 associated with Smith-Magenis syndrome;Slager;Nat Genet,2003
5. Circadian rhythm abnormalities of melatonin in Smith-Magenis syndrome;Potocki;J Med Genet,2000
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