Nothing is simple in colour vision and genetics

Clinical and Experimental Optometry

Volumn 89, Issue 3, 2006, Pages 185-186

  Harris, Ross W ^a   Cole, Barry L ^a  

^a UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 35448991305     PISSN: 08164622     EISSN: 14440938     Source Type: Journal    
DOI: 10.1111/j.1444-0938.2006.00043.x     Document Type: Letter

References (9)

1. Harris RW, Cole BL. Diagnosing protan heterozygosity using the Medmont C-100 colour vision test Clin Exp Optom 2005;88:240-247.
2. Sharpe LT, Stockman A, Jägle H, Nathans J. Opsin genes, cone photopigments, color vision and color blindness. In: Gegenfurtner KR, Sharpe LT, eds. Color Vision: From Genes to Perception. New York: Cambridge University Press, 1999.
3. Pickford RW. Individual Differences in Colour Vision. London: Routledge and Kegan Paul, LTD, 1951. p 76.
4. Brunner W. Ueber den Vererbungsmodus der verschiedenen Typen der angeborenen Rotgruenblindheit Albrecht von Graefes Arch Ophthalmol 1932;124:1-52.
5. Kondo T. Untersuchungen bei angeborenen Farbensinn-Anomalien. Ueber das Zustandekommen und Wesen der angeborenen Farbensinn-Anomalien. Acta Soc Ophthalmol Jap 1941;45:659.
6. Franceschetti A, Klein D. Two families with parents of different types of red-green blindness Acta genet statist med 1957;7:255-259.
7. Vanderdonck R, Verriest G. Femme protanomale et heterozygote mixte (genes de la protanomalie et de la deuteranopie en position de repulsion) ayant deux fils deuteranopes, un fils protanomal et deux fils normaux Biotypologie 1960;21:110-120.
8. Hunt DM, Dulai KS, Bowmaker JK, Mollon JD. The chemistry of John Dalton's color blindness Science 1995;267:984-988.
9. Harris RW, Cole BL. Diagosing protan heterozygosity using the Medmont C-100 colour vision test Clin Exp Optom 2005;88:240-247.