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A New Rett Syndrome Family Consistent with X-Linked Inheritance Expands the X Chromosome Exclusion Map

N. Carolyn Schanen, E. Jill Dahle, Fiorentino Capozzoli, Vanja A. Holm, Huda Y. Zoghbi, Uta Francke

The American Journal of Human Genetics · 1997 · 115 citations · 24 references

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24

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.

R.Cutler Allen, Huda Y. Zoghbi, A. Moseley et al. · PubMed · 1992 · 1.7K citations

, , +14

A second-generation linkage map of the human genome

Jean Weissenbach, Gàbor Gyapay, Colette Dib et al. · Nature · 1992 · 1.7K citations

, , +14

Rett's Syndrome: Prevalence and Impact on Progressive Severe Mental Retardation in Girls

Bengt Hagberg · Acta Paediatrica · 1985 · 281 citations

, , +8

Heritability of X chromosome--inactivation phenotype in a large family.

Anna K. Naumova, Robert M. Plenge, Lynne M. Bird et al. · PubMed · 1996 · 176 citations

, , +11

Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females.

Elena Pegoraro, R. Neil Schimke, Kiichi Arahata et al. · PubMed · 1994 · 142 citations

, , +11