Congenital Stationary Night Blindness
- 1 December 1994
- book chapter
- Published by Taylor & Francis
- p. 277-301
- https://doi.org/10.1201/b14734-12
Abstract
No abstract availableThis publication has 38 references indexed in Scilit:
- Linkage analysis in X-linked congenital stationary night blindnessGenomics, 1992
- Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7Genomics, 1992
- Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosomeHuman Genetics, 1985
- BASIC PRINCIPLES OF CLINICAL ELECTRORETINOGRAPHYRetina, 1985
- Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28Nature, 1984
- Discrete Visual Defects in Pearl Mutant MiceScience, 1983
- Temporal Aspects of the Electroretinogram in Sector Retinitis PigmentosaArchives of Ophthalmology (1950), 1971
- Temporal Aspects of the ElectroretinogramArchives of Ophthalmology (1950), 1969
- Constatations histologiques dans l’amaurose infantile de Leber et dans diverses formes d’héméralopieOphthalmologica, 1963
- Zur Vererbung der Hemeralopia hereditaria und tapeto-retinalen DegenerationOphthalmologica, 1946