An Electroretinographic and Molecular Genetic Study of X-Linked Cone Degeneration
- 1 November 1989
- journal article
- research article
- Published by Elsevier in American Journal of Ophthalmology
- Vol. 108 (5) , 540-547
- https://doi.org/10.1016/0002-9394(89)90431-5
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Dystrophin abnormalities in Duchenne/Becker muscular dystrophyNeuron, 1989
- Report of the committee on the genetic constitution of the X and Y chromosomesCytogenetic and Genome Research, 1987
- Electroretinograms in Carriers of Blue Cone MonochromatismAmerican Journal of Ophthalmology, 1986
- Molecular Genetics of Inherited Variation in Human Color VisionScience, 1986
- Molecular Genetics of Human Color Vision: The Genes Encoding Blue, Green, and Red PigmentsScience, 1986
- Color Plates to Help Identify Patients with Blue Cone MonochromatismAmerican Journal of Ophthalmology, 1983
- Rod-Cone Interaction in the Distal Human RetinaScience, 1981
- Sex-difference in progressive cone dystrophy. IOphthalmic Paediatrics and Genetics, 1981
- Sex-difference in progressive cone dystrophy. IIOphthalmic Paediatrics and Genetics, 1981
- Gene Action in the X-chromosome of the Mouse (Mus musculus L.)Nature, 1961