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7. [STUDIES ON THE OCCUPATIONAL ABILITY OF PERSONS WITH CONGENITAL COLOR BLINDNESS]. KUWABARA T; YASUI K; OHNO Y Rinsho Ganka; 1964 Mar; 18():315-9. PubMed ID: 14142920 [No Abstract] [Full Text] [Related]
8. [Early detection of color blindness from the viewpoint of occupational medicine with various references to internistic and human genetic symptom complexes]. Ebéné RT Fortschr Med; 1983 Jan; 101(3):51-4. PubMed ID: 6600702 [TBL] [Abstract][Full Text] [Related]
9. Minor colour vision defects: sib-sib correlations and relation to unique colours. De Bie S; Wilmet J; Verriest G; Pierart P Bull Soc Belge Ophtalmol; 1987; 224():81-93. PubMed ID: 3509910 [No Abstract] [Full Text] [Related]
10. Defective color vision and occupational adaptability. Ichikawa H; Hukami K; Majima A Ophthalmologica; 1969; 158 Suppl():428-33. PubMed ID: 5307971 [No Abstract] [Full Text] [Related]
11. Colour vision defects and gene flow in Nigerians. Odeigah PG; Okon EE East Afr Med J; 1986 Oct; 63(10):666-71. PubMed ID: 3493131 [No Abstract] [Full Text] [Related]
12. Genetics and physiology of colour vision ("my story on colour vision genetics and physiology"). Waaler GH Acta Ophthalmol Suppl; 1973; ():1-75. PubMed ID: 4356807 [No Abstract] [Full Text] [Related]
13. [Color vision defects in endogenous depression]. Heim M; Morgner J Psychiatr Prax; 1997 Mar; 24(2):73. PubMed ID: 9190613 [TBL] [Abstract][Full Text] [Related]
14. An advisory clinic for colour defective children. Taylor WO Trans Ophthalmol Soc U K (1962); 1966; 86():591-607. PubMed ID: 5297477 [No Abstract] [Full Text] [Related]
15. [Genetics of congenital color vision defects. I. Common types of color blindness]. Krawczyński MR Klin Oczna; 1995; 97(1-2):34-8. PubMed ID: 7637311 [TBL] [Abstract][Full Text] [Related]
16. Increment spectral sensitivity of hemizygotes and heterozygotes for different classes of colour vision. de Vries-de Mol EC; Went LN; van Norren D; Pols LC Mod Probl Ophthalmol; 1978; 19():224-8. PubMed ID: 310035 [No Abstract] [Full Text] [Related]
17. Color vision. Plunkett ER J Occup Med; 1970 Dec; 12(12):524-5. PubMed ID: 5312861 [No Abstract] [Full Text] [Related]
18. Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study. Quiros PA; Torres RJ; Salomao S; Berezovsky A; Carelli V; Sherman J; Sadun F; De Negri A; Belfort R; Sadun AA Br J Ophthalmol; 2006 Feb; 90(2):150-3. PubMed ID: 16424523 [TBL] [Abstract][Full Text] [Related]
19. Red-green colour blindness in the Tormes-Alberche Valley (Avila-Central Spain). Cabrero FJ; Ortiz MA; Mesa MS; Fuster V; Moral P Anthropol Anz; 1997 Dec; 55(3-4):295-301. PubMed ID: 9468757 [TBL] [Abstract][Full Text] [Related]