Neither uniparental disomy nor skewed X-inactivation explains Rett syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb03889.x/fullpdf
Reference28 articles.
1. Segregation analysis of the X chromosome in a family with Rett syndrome in two generations;Anvret;Am J Med Genet,1990
2. Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations;Archidiacono;Hum Genet,1991
3. Parental origin of the X-chromosomes in Rett syndrome;Benedetti;Am J Med Genet,1992
4. Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): correlation with X-inactivation status;Boyd;Genomics,1990
5. Localisation of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation;Brown;Am J Hum Genet,1990
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1. Earlier finishing of Xp21.2 subband replication of the inactive X chromosome in Rett syndrome girl but not in her 47,XXX mother;Clinical Genetics;2008-06-28
2. A comparative study of X-inactivation in Rett syndrome probands and control subjects;Clinical Genetics;2008-06-28
3. Review and meta-analysis of systematic searches for uniparental disomy (UPD) other than UPD 15;American Journal of Medical Genetics;2002-08-26
4. Genetic basis of rett syndrome;Mental Retardation and Developmental Disabilities Research Reviews;2002
5. Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome;Brain and Development;2001-12
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