TheMECP2duplication syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference53 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999
2. Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplication;Ariani;Hum Mutat,2004
3. Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair;Bauters;Genome Res,2008
4. Mutation analysis of the coding sequence of the MECP2 gene in infantile autism;Beyer;Hum Genet,2002
5. Identification of MeCP2 mutations in a series of females with autistic disorder;Carney;Pediatr Neurol,2003
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