Literature DB >> 13364167

Combined forms of congenital colour defects; a pedigree with atypical total colour blindness.

R A CRONE.   

Abstract

Entities:  

Keywords:  COLOR VISION; HEREDITY

Mesh：

Year:  1956        PMID： 13364167      PMCID： PMC1324646          DOI： 10.1136/bjo.40.8.462

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN： 0007-1161            Impact factor:   4.638


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  7 in total

1.  Clinical study of colour vision.

Authors:  R A CRONE
Journal:  Br J Ophthalmol       Date:  1955-03       Impact factor: 4.638

2.  The familial distribution of congenital tritanopia, with some remarks on some similar conditions.

Authors:  H KALMUS
Journal:  Ann Hum Genet       Date:  1955-08       Impact factor: 1.670

3.  New means of studying color blindness and normal foveal color vision, with some results and their genetical implications.

Authors:  G L WALLS; R W MATHEWS
Journal:  Publ Psychol       Date:  1952-04-29

4.  Cone-monochromatism.

Authors:  R A WEALE
Journal:  J Physiol       Date:  1953-09       Impact factor: 5.182

5.  Defects of the colour-sense mechanism as indicated by the accommodation reflex.

Authors:  E F FINCHAM
Journal:  J Physiol       Date:  1953-09       Impact factor: 5.182

6.  Typical total color blindness reinterpreted.

Authors:  G L WALLS; G G HEATH
Journal:  Acta Ophthalmol (Copenh)       Date:  1954

7.  The characteristics of tritanopia.

Authors:  W D WRIGHT
Journal:  J Opt Soc Am       Date:  1952-08
  7 in total
  2 in total

1.  Diagnostic tests for colour vision.

Authors:  W D WRIGHT
Journal:  Ann R Coll Surg Engl       Date:  1957-03       Impact factor: 1.891

Review 2.  The cone dysfunction syndromes.

Authors:  M Michaelides; D M Hunt; A T Moore
Journal:  Br J Ophthalmol       Date:  2004-02       Impact factor: 4.638
  2 in total

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