1. Choroideremia and deafness with stapes fixation: a contigous gene deletion syndrome in Xq21;Merry, D.E.; Leslo, J.G.; Sosnoski, D.M.;Am _7 Humn Genet,1989
2. Choroideremia: further evidence for assignment of the locus to Xql 3Xq21;Schwartz, M.; Rosenberg, T.; Niebuhr, E.,1986
3. Paracentric inversion X(q21.2q24) associated with mental retardation in males and normal ovarian function in females;Abeliovitch, D.; Dagan, J.; Kimchi-Sarfati, C.; Zlotogora, J.;Am]_Med Genet,1995
4. Growth hormone deficiency and empty sella syndrome in a boy with dup(X)(q13.3-q21.2);Yokoyama, Y.; Narahara, K.; Tsuji, K.;Anm Med Genet,1992
5. Isolation of anonymous sequences from within a submicroscopic X-chromosome deletion in a patient with choroideremia, deafness;Nussbaum, R.L.; Lesko, J.G.; Lewis, R.A.; Ledbetter, S.A.; Ledbetter, D.H.,1987