The biological functions of the methyl-CpG-binding protein MeCP2 and its implication in Rett syndrome
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health
Reference64 articles.
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3. Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28;Sirianni;Am J Hum Genet,1998
4. Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28;Webb;J Med Genet,1998
5. Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq;Xiang;J Med Genet,1998
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