1. Linkage analysis in X-linked congenital stationary night blindness;Aldred;Genomics,1992
2. Aldred, M.A., Teague, P. W., Jay, M., Bundey, S., Redmond, R. M., Jay, B., Bird, A. C., Bhattacharya, S. S., and Wright, A. F. (1993). Retinitis pigmentosa families showing apparent X-linked inheritance but unlinked to RP2 or RP3. Submitted for publication.
3. Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis;Alitalo;Am. J. Hum. Genet.,1991
4. Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19;Al-Maghtheh;Hum. Mol. Genet.,1994
5. ROM1: A candidate gene for autosomal dominant retinitis pigmentosa (ADRP) and Best vitelliform macular dystrophy;Bascom;Am. J. Hum. Genet.,1992