Related Experiment Videos
A family with congenital deutan and tritan defects
Modern Problems in Ophthalmology
|January 1, 1976
Abstract:
A family has been found with deuteranopia and a tritan defect which is not sex-linked. It is proposed that there is also an autosomal dominant gene for tritan defects showing variable expressivity.
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Inhibition of HERV-K (HML-2) in amyotrophic lateral sclerosis patients on antiretroviral therapy.
Journal of the neurological sciences·2021
Detection of first gammaherpesvirus sequences in Central African bats.
New microbes and new infections·2020
A Health Services Research Agenda for Bariatric Surgery Within the Veterans Health Administration.
Journal of general internal medicine·2017
Scleral buckling in 2 1/2 to 11-month-old premature infants with retinal detachment associated with acute retrolental fibroplasia.
Modern problems in ophthalmology·1979
[Treatment of complications of venous retinal thromboses with argon laser].
Modern problems in ophthalmology·1979
Prophylactic photocoagulation of the fellow eye in exudative senile maculopathy. A preliminary report.
Modern problems in ophthalmology·1979
Retinal telangiectasias associated with longstanding retinal detachment as a prognostic sign.
Modern problems in ophthalmology·1979
Central serous retinopathy. A generalized disease of the pigment epithelium.
Modern problems in ophthalmology·1979
[Postoperative choroidal detachment and chorioretinal surgery].
Modern problems in ophthalmology·1979
Allele-specific expression modulates the immunological and cis-regulatory landscape of Parkinson's Disease.
Computers in biology and medicine·2026
Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort.
The British journal of dermatology·2026
Beyond in silico prediction: multi-omics to identify a pathogenic deep intronic HNRNPK variant in Au-Kline syndrome.
Journal of human genetics·2026
Phenotypes of Hereditary Diseases Associated With Rauch-Steindl Syndrome.
Human mutation·2026
Multi-omics Mendelian Randomization Prioritizes Neutrophil Extracellular Trap-related Genes Associated with Atrial Fibrillation Risk.
Endocrine, metabolic & immune disorders drug targets·2026
Developmental and cellular vulnerabilities underlie genetic architecture of schizophrenia.
Molecular psychiatry·2026