These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
9. Colour vision in a pedigree with autosomal dominant optic atrophy. Ohba N, Imamura PM, Tanino T. Mod Probl Ophthalmol; 1976 Jul 01; 17():315-9. PubMed ID: 1085884 [No Abstract] [Full Text] [Related]
10. [Abnormal color vision in the light of examinations of school children]. Goncerzewicz M, Krawczyński M, Suchocka-Luczak S. Pediatr Pol; 1971 Mar 01; 46(3):327-31. PubMed ID: 5314000 [No Abstract] [Full Text] [Related]
12. Recent cases of acquired color vision deficiencies. François J, Verriest G. Ann Ocul (Paris); 1968 Nov 01; 201(11):1097-114. PubMed ID: 5314834 [No Abstract] [Full Text] [Related]
13. A practical guide for colour-vision examination: report of the Standardization Committee of the International Research Group on Colour-Vision Deficiencies. Birch J. Ophthalmic Physiol Opt; 1985 Nov 01; 5(3):265-85. PubMed ID: 3876538 [Abstract] [Full Text] [Related]
18. Genealogical studies on interesting families of defective colour vision discovered by a mass examination in Japan and Formosa. Ichikawa H, Majima A. Mod Probl Ophthalmol; 1974 Nov 01; 13(0):265-71. PubMed ID: 4548143 [No Abstract] [Full Text] [Related]