1. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation;Allen;Am J Hum Genet,1992
2. Parental origin of the X chromosomes in Rett syndrome;Benedetti;Am J Med Genet,1992
3. Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): correlation with X-inactivation status;Boyd;Genomics,1990
4. X-inactivation in Rett syndrome;Camus;Am J Med Genet,1994
5. Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girl;Clarke;Am J Hum Genet,1991