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2. Combined forms of congenital colour defects; a pedigree with atypical total colour blindness. CRONE RA Br J Ophthalmol; 1956 Aug; 40(8):462-72. PubMed ID: 13364167 [No Abstract] [Full Text] [Related]
3. An estimate from pedigree data of the gene frequency for colour blindness. KNOX G Br J Prev Soc Med; 1958 Oct; 12(4):193-6. PubMed ID: 13638529 [No Abstract] [Full Text] [Related]
4. Colour blindness and the Duchenne-type muscular dystrophy. PHILIP U; SMITH CA; WALTON JN Ann Hum Genet; 1956 Nov; 21(2):155-8. PubMed ID: 13373181 [No Abstract] [Full Text] [Related]
5. P.T.C. thresholds, colour vision and blood factors of Brazilian Indians. I. Kaingangs. FERNANDES JL; JUNQUEIRA PC; KALMUS H; OTTENSOOSER F; PASQUALIN R; WISHART P Ann Hum Genet; 1957 Oct; 22(1):16-21. PubMed ID: 13488180 [No Abstract] [Full Text] [Related]
6. P.T.C. thresholds, colour vision and blood factors of Brazilian Indians. II. Carajas. JUNQUEIRA PC; KALMUS H; WISHART P Ann Hum Genet; 1957 Oct; 22(1):22-5. PubMed ID: 13488181 [No Abstract] [Full Text] [Related]
7. New means of studying color blindness and normal foveal color vision, with some results and their genetical implications. WALLS GL; MATHEWS RW Publ Psychol; 1952 Apr; 7(1):1-172. PubMed ID: 13179377 [No Abstract] [Full Text] [Related]
8. Tests for partial sex-linkage in total color-blindness. TANAKA K Acta Genet Med Gemellol (Roma); 1957 Jan; 6(1):45-51. PubMed ID: 13394078 [No Abstract] [Full Text] [Related]
10. Two families with parents of different types of red-green blindness. FRANCESCHETTI A; KLEIN D Acta Genet Stat Med; 1957; 7(2):255-9. PubMed ID: 13469157 [No Abstract] [Full Text] [Related]
11. The familial distribution of congenital tritanopia, with some remarks on some similar conditions. KALMUS H Ann Hum Genet; 1955 Aug; 20(1):39-56. PubMed ID: 13249225 [No Abstract] [Full Text] [Related]
12. Hereditary optic atrophy with dominant transmission; with special reference to the associated color-sense disorder. JAEGER W Albrecht Von Graefes Arch Ophthalmol; 1954; 155(5):457-84. PubMed ID: 13217987 [No Abstract] [Full Text] [Related]
13. On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies. WALTON JN; RACE RR; PHILIP U Ann Hum Genet; 1955 Aug; 20(1):1-38. PubMed ID: 13249224 [No Abstract] [Full Text] [Related]
14. [Congenital atrophy of the optic nerve with disorders in determination of colors; recessive hereditary trait]. WAARDENBURG PJ J Genet Hum; 1956 Aug; 5(2):99-105. PubMed ID: 13367370 [No Abstract] [Full Text] [Related]
15. Effect of migration on some genetical characters in six endogamous groups in India. SIRSAT SM Ann Hum Genet; 1956 Nov; 21(2):145-54. PubMed ID: 13373180 [No Abstract] [Full Text] [Related]
16. Colour and colour vision in animals. CARTER GS Nature; 1948 Oct; 162(4120):600. PubMed ID: 18888143 [No Abstract] [Full Text] [Related]
17. Inheritance of dun, brown and brindle colour in cattle. BERGE S Heredity (Edinb); 1949 Aug; Pt. 2 3():195-204. PubMed ID: 18143386 [No Abstract] [Full Text] [Related]
18. The application of spectrophotometry to the study of skin colour inheritance. HARRISON GA; OWEN JJ Acta Genet Stat Med; 1956-1957; 6(3):481-4; discussion, 484-5. PubMed ID: 13434739 [No Abstract] [Full Text] [Related]
19. Rapid testing of monocular and binocular colour vision with pseudo-isochromatic plates and diploscope. WAARDENBURG PJ Ophthalmologica; 1951 Dec; 122(6):389-90. PubMed ID: 14899877 [No Abstract] [Full Text] [Related]
20. Colour vision of Buganda Africans. SIMON K East Afr Med J; 1951 Feb; 28(2):75-9. PubMed ID: 14840361 [No Abstract] [Full Text] [Related] [Next] [New Search]