Log in or create a free account to read this content
Gain free access to this article, as well as selected content from this journal and more on nature.com
or
References
Nelson LB, Spaeth GL, Margo CE, Laird J . Aniridia: a review. Surv Ophthalmol 1984;28:621–42.
Fraumeni JF, Glan AG . Wilms' tumour and congenital aniridia. JAMA 1968;206:825–8.
Ton CCT, et al. Positional cloning and characterisation of a paired box and homeobox-containing gene from the aniridia region. Cell 1991;67:1059–74.
Davis A, Cowell JK . Mutations in the PAX6 gene in patients with hereditary aniridia. Hum Mol Genet 1993;2:2093–7.
Hanson MI, et al. PAX6 mutations in aniridia. Hum Mol Genet 1993;2:915–20.
Berry AC, et al. Monozygotic twins discordant for Wiedeman-Beckwith syndrome and the implications for genetic counselling. J Med Genet 1980;17:136–8.
Olney AH, et al. Beckwith-Wiedeman syndrome in discordant monozygotic twins. Am J Med Genet 1988;29:491–9.
Lubinsky MS, Hall J . Genomic imprinting, monozygous twinning and X inactivation. Lancet 1991;237:1288.
Jinno Y, et al. Mosaic and polymorphic imprinting of the WT1 gene in humans. Nature Genet 1994;6:305–7.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Sadiq, S., Sharif, A. & Gregson, R. Aniridia in only one identical twin. Eye 10, 392–394 (1996). https://doi.org/10.1038/eye.1996.79
Issue date:
DOI: https://doi.org/10.1038/eye.1996.79