1. X-X translocation in a patient with gonadal dysgenesis and the problem of phenotype-karyotype correlations;Mirzayants, G.G.; Baranovskaya, L.I.;Humiii Genet,1978
2. Evidence for X/X chromosome translocation in humans;Sinha, A.K.; Nora, J.J.;Ann Hum Genet
3. X-inactivation in man: a woman with t(Xq-; 12q+);Sarto, G.E.; Therman, E.; Patau, K.;Amn J Hum Genet,1973
4. A case of 46, X, t(X; X)(pter-q27::q27 -pter)/47, X, t,(X; X)(pter -, q27::q27, pter), + mar/48, XX, t(X; X)(pterq27::q27-pter);Nielsen, J.; Homma, A.; Christiansen, F.; Rasmussen, K.; Saldana-Garcia, P.;Ann Genet (Paris); and functionally monocentric translocation X,1977
5. Duplication deficiency of an X-chromosome with and without 45, X mosaicism in three girls;Schwanitz, G.; Tietze, H.U.; Pfeiffer, R.A.; Grosse, K.P.; Beker, H.; Eger, H.;Acta Genet Med Gemnellol,1977