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8. Polymorphism in the number of genes encoding long-wavelength-sensitive cone pigments among males with normal color vision. Neitz M; Neitz J; Grishok A Vision Res; 1995 Sep; 35(17):2395-407. PubMed ID: 8594809 [TBL] [Abstract][Full Text] [Related]
9. Adrenoleukodystrophy: overlapping deletions point to a gene location in Xq28. Sack GH; Morrell JC Biochem Biophys Res Commun; 1993 Mar; 191(3):955-60. PubMed ID: 8466536 [TBL] [Abstract][Full Text] [Related]
10. [Genetics of congenital color vision defects. II. Rare types of color blindness]. Krawczyński MR Klin Oczna; 1995; 97(1-2):39-43. PubMed ID: 7637312 [TBL] [Abstract][Full Text] [Related]
11. Novel form of a single X-linked visual pigment gene in a unique dichromatic color-vision defect. Hayashi T; Kubo A; Takeuchi T; Gekka T; Goto-Omoto S; Kitahara K Vis Neurosci; 2006; 23(3-4):411-7. PubMed ID: 16961974 [TBL] [Abstract][Full Text] [Related]
13. Photopigment basis for dichromatic color vision in the horse. Carroll J; Murphy CJ; Neitz M; Hoeve JN; Neitz J J Vis; 2001; 1(2):80-7. PubMed ID: 12678603 [TBL] [Abstract][Full Text] [Related]
14. Is colour vision possible with only rods and blue-sensitive cones? Reitner A; Sharpe LT; Zrenner E Nature; 1991 Aug; 352(6338):798-800. PubMed ID: 1881435 [TBL] [Abstract][Full Text] [Related]
15. Adrenoleukodystrophy in a mother and son. Simpson RH; Rodda J; Reinecke CJ J Neurol Neurosurg Psychiatry; 1987 Sep; 50(9):1165-72. PubMed ID: 2822858 [TBL] [Abstract][Full Text] [Related]
16. Variations of colour vision in a New World primate can be explained by polymorphism of retinal photopigments. Mollon JD; Bowmaker JK; Jacobs GH Proc R Soc Lond B Biol Sci; 1984 Sep; 222(1228):373-99. PubMed ID: 6149558 [TBL] [Abstract][Full Text] [Related]
17. Trichromatic colour vision in New World monkeys. Jacobs GH; Neitz M; Deegan JF; Neitz J Nature; 1996 Jul; 382(6587):156-8. PubMed ID: 8700203 [TBL] [Abstract][Full Text] [Related]
18. The molecular basis of variation in human color vision. Deeb SS Clin Genet; 2005 May; 67(5):369-77. PubMed ID: 15811001 [TBL] [Abstract][Full Text] [Related]