1. Methylation of Hpall and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor because such an event can be a mendelian trait in a few families" and approximately 10% of normal females have shown this pattern by the gene Hum correlates with X chromosome Genet;Allen, R.C.; Zoghbi, H.Y.; Moseley, A.B.; Rosenblatt, H.M.; Belmont, J.W.,1992
2. Catalogue of unbalanced chromosome aberrations in man;Schinzel, A.,1983
3. Proximal duplication of the long arm of chromosome 10 afterwards the somatic cells with an inactive (lOql 1.2-*10q22): a distinct clinical entity;Fryns, J.P.; Kleczkowska, A.; Igodt-Ameye, L.; Van den Berghe, H.;Clin Genet,1987
4. Deletions Xq and growth deficit: a review;Geerkens, C.; Just, W.; Vogel, W.;Am J Med Genet,1994
5. Skewed X-inactivation can be karyotype would have been more unbalanced inherited as a Mendelian trait in humans;Hoffman, E.P.; Pegoraro, E.;Am; Hum Genet and potentially lethal (monosomy of Xq26-*Xqter and trisomy of 1 Oq2 1 -*1 Oqter,1995