References
- Bhattacharya S. S., Wright A. F., Clayton J. F., Price W. H., Phillips C. I., McKeown C. M. E., Jay M., Bird A. C., Pearson P. L., Southern E. M., Evans H. J. Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28. Nature 1984; 309: 253–255
- Clayton J. A multi-point linkage analysis program for X-linked disorders, with the example of Duchenne muscular dystrophy and seven DNA probes. Hum. Genet, in press
- Cooke H., Bhattacharya S. S., Fantes J. A., Green D. K., Evans H. J. Preparation of X-chromosome specific probes from a flow sorted library. Cytogenet. Cell. Genet. 1985; 40: 607
- De Martinville B., Kunkel L. M., Bruns G., Morle F., Koenig M., Mandel J. L., Horwich A., Latt S. A., Gusella J. F., Housman D., Franke U. Localisation of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus. Amer. J. hum. Genet. 1985; 37: 235–249
- Harris G. S., Miller J. R. Choroideremia: visual defects in a heterozygote. Arch. Ophthal. 1968; 80: 423–429
- Kunkel L. M., Tantravahi U., Eisenhard M., Latt S. A. Regional localisation on the human X of DNA segments cloned from flow sorted chromosomes. Nucleic Acids Res. 1982; 10: 1557–1558
- Kurstgens J. H. Choroideremia and gyrate atrophy of the choroid and retina. Docum. ophthal. (The Hague) 1965; 19: 1–122
- McCulloch C., McCulloch R. J. P. A hereditary and clinical study of choroideremia. Trans. Amer. Acad. Ophthal. Otolaryngol. 1948; 52: 160–190
- Nussbaum R. L., Lewis R. A., Lesko J. G., Ferrell R. Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at Xq13–21. Amer. J. hum. Genet. 1985; 37: 565–575
- Page D. C., De La Chapelle A. Parental origin of X chromosome in XX males determined using restriction fragment length polymorphisms. Amer. J. hum. Genet. 1984; 36: 565–575
- Pameyer J. K., Waardenburg P. G., Henkes H. E. Choroideremia. Brit. J. Ophthal. 1960; 44: 724–738
- Sorsby A., Franceschetti A., Joseph R., Davey J. B. Choroideremia, clinical and genetic aspects. Brit. J. Ophthal. 1952; 36: 547–581
- Wieacker P., Davies K. E., Cooke H. J., Pearson P. L., Williamson R., Bhattacharya S., Zimmer J., Ropers H.-H. Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids. Amer. J. hum. Genet. 1984; 36: 265–276
- Willard H. F., Skolnick M. H., Pearson P. L., Mandel J.-L. Report of the committee on human gene mapping by recombinant DNA techniques. Cytogenet. Cell. Genet. 1985; 40: 360–489