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22. 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 [Abstract] [Full Text] [Related]
29. [Genetic study of 4 cases of testicular feminization in a sibship with 4 cases of dyschromatopsia]. Legueult LC, Ropartz C. Ann Genet; 1972 Dec 28; 15(4):219-23. PubMed ID: 4539480 [No Abstract] [Full Text] [Related]
30. [Dyschromatopsy in twins]. Kloucek F, Kubicková Z. Sb Lek; 1971 Mar 28; 73(3):57-63. PubMed ID: 5313898 [No Abstract] [Full Text] [Related]
31. A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation. Pembrey ME, Winter RM, Davies KE. Am J Med Genet; 1985 Aug 28; 21(4):709-17. PubMed ID: 4040705 [Abstract] [Full Text] [Related]
32. Some remarks on the clinical and genetic puzzle of Leber's optic neuritis. Waardenburg PJ. J Genet Hum; 1969 Oct 28; 17(3):479-95. PubMed ID: 5387423 [No Abstract] [Full Text] [Related]
37. [Tritan type congenital anomalies and acquired color vision defects. Results of a genetic survey in an isolated group, the Kel Kummer]. Roth A, Chaventré-Mano A, Chaventré A. Bull Mem Soc Fr Ophtalmol; 1980 Oct 28; 92():336-44. PubMed ID: 6971685 [No Abstract] [Full Text] [Related]
38. [Quantitative test of color vision in healthy Chinese and genetic carriers of color deficiency]. Chang J. Zhonghua Yan Ke Za Zhi; 1982 Jul 28; 18(4):242-4. PubMed ID: 6816554 [No Abstract] [Full Text] [Related]
40. [Congenital dyschromatopsia in Italy. Study of a sample of 2967 subjects]. Del Giudice R, Planner- Terzaghi A, Stella C. Riv Med Aeronaut Spaz; 1985 Jul 28; 52(2):151-5. PubMed ID: 3880498 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]