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2. Chromaticity discrimination in protan and deutan heterozygotes. Verriest G Mod Probl Ophthalmol; 1974; 13(0):262-4. PubMed ID: 4548142 [No Abstract] [Full Text] [Related]
3. Color discrimination in carriers of color deficiency. Hood SM; Mollon JD; Purves L; Jordan G Vision Res; 2006 Sep; 46(18):2894-900. PubMed ID: 16690099 [TBL] [Abstract][Full Text] [Related]
4. [The phenotype of heterozygotic females in congenital red-green color blindness (author's transl)]. Fahrenkamp-Richner K Klin Monbl Augenheilkd; 1976 Jan; 168(1):128-34. PubMed ID: 1086400 [TBL] [Abstract][Full Text] [Related]
5. Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy. Ventura DF; Gualtieri M; Oliveira AG; Costa MF; Quiros P; Sadun F; de Negri AM; Salomão SR; Berezovsky A; Sherman J; Sadun AA; Carelli V Invest Ophthalmol Vis Sci; 2007 May; 48(5):2362-70. PubMed ID: 17460303 [TBL] [Abstract][Full Text] [Related]
6. Silent substitution tests like the OSCAR and the Medmont C100 can identify protan and deutan carriers of abnormal colour vision. Robbins HG Clin Exp Optom; 2005 Nov; 88(6):426-7. PubMed ID: 16329753 [No Abstract] [Full Text] [Related]
7. Normality of colour vision in a compound heterozygous female carrying protan and deutan defects. Tait DM; Carroll J Clin Exp Optom; 2009 Jul; 92(4):356-61. PubMed ID: 19473349 [TBL] [Abstract][Full Text] [Related]
8. Non-allelic compounds of protan and deutan deficiencies. Jaeger W; Lauer HJ Mod Probl Ophthalmol; 1976; 17():121-30. PubMed ID: 1085856 [No Abstract] [Full Text] [Related]
10. [Color vision test for detection and evaluation of dyschromatopsia]. Ionica V; Gastaud P J Fr Ophtalmol; 1996; 19(11):679-88. PubMed ID: 9033889 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Variant phenotypes of incomplete achromatopsia in two cousins with GNAT2 gene mutations. Rosenberg T; Baumann B; Kohl S; Zrenner E; Jorgensen AL; Wissinger B Invest Ophthalmol Vis Sci; 2004 Dec; 45(12):4256-62. PubMed ID: 15557429 [TBL] [Abstract][Full Text] [Related]
13. [The progeny of the two protan and deutan families described by Franceschetti and Klein (1949, 1956), one generation later. Genealogy, color vision and genomic DNA]. Roth A; Klein D; Paccolat F; Hermès D; Pelizzone M; Mandel JL; Feil R Ophtalmologie; 1989; 3(4):275-8. PubMed ID: 2641134 [TBL] [Abstract][Full Text] [Related]
14. Frequencies of protan and deutan alleles in some Israeli communities and a note on the selection-relaxation hypothesis. Adam A; Doron D; Modan R Am J Phys Anthropol; 1967 May; 26(3):297-305. PubMed ID: 5298526 [No Abstract] [Full Text] [Related]
15. An informative large pedigree with four compound hemizygotes of three combinations of deutan and protan genes. Arias S; Rodríguez A Acta Cient Venez; 1973; 24(2):44-52. PubMed ID: 4549004 [No Abstract] [Full Text] [Related]
16. [Quantitative test of color vision in healthy Chinese and genetic carriers of color deficiency]. Chang J Zhonghua Yan Ke Za Zhi; 1982 Jul; 18(4):242-4. PubMed ID: 6816554 [No Abstract] [Full Text] [Related]
17. [Characteristics of genetic carriers of congenital color vision defects. (5) Abnormalities of cone photopigments in proto-carriers]. Yasuma T; Tokuda H Nippon Ganka Gakkai Zasshi; 1982; 86(6):601-6. PubMed ID: 6982608 [No Abstract] [Full Text] [Related]
18. THE RED-LIGHT ABSOLUTE THRESHOLD IN HETEROZYGOTE PROTAN CARRIERS. POSSIBLE GENETIC IMPLICATIONS. KRILL AE; BEUTLER E Invest Ophthalmol; 1964 Feb; 3():107-18. PubMed ID: 14121141 [No Abstract] [Full Text] [Related]
19. Polymorphisms of red-green vision in some populations of Southern Africa. Adam A Am J Phys Anthropol; 1980 Sep; 53(3):339-46. PubMed ID: 6970528 [TBL] [Abstract][Full Text] [Related]
20. [Color vision defects in alcoholic women and their relatives]. Cruz-Coke R; Rivera L; Kattan L; Mardones J Rev Med Chil; 1971 Feb; 99(2):118-24. PubMed ID: 5314541 [No Abstract] [Full Text] [Related] [Next] [New Search]