Literature DB >> 13179377

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

G L WALLS, R W MATHEWS.   

Abstract

Entities:  

Keywords:  COLOR VISION; HEREDITY

Mesh:

Year:  1952        PMID: 13179377

Source DB:  PubMed          Journal:  Publ Psychol


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  13 in total

1.  Color theory and abnormal redgreen vision.

Authors:  L M HURVICH; D JAMESON
Journal:  Doc Ophthalmol       Date:  1962       Impact factor: 2.379

2.  Diagnostic tests for colour vision.

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

3.  The Cunier pedigree of color blindness.

Authors:  C STERN; G L WALLS
Journal:  Am J Hum Genet       Date:  1957-12       Impact factor: 11.025

4.  A physiological basis for human colour vision in the central fovea.

Authors:  E N WILLMER
Journal:  Doc Ophthalmol       Date:  1955       Impact factor: 2.379

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

Authors:  R A CRONE
Journal:  Br J Ophthalmol       Date:  1956-08       Impact factor: 4.638

6.  Cone-monochromatism.

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

7.  Sex chromatin and gene action in the mammalian X-chromosome.

Authors:  M F LYON
Journal:  Am J Hum Genet       Date:  1962-06       Impact factor: 11.025

8.  New families, one with two recombinants for estimation of recombination between the deutan and protan loci.

Authors:  S Arias; A Rodríguez
Journal:  Humangenetik       Date:  1972

9.  Prereceptor colour vision distortions in protanomalous trichromacy.

Authors:  M Alpern; S Torii
Journal:  J Physiol       Date:  1968-10       Impact factor: 5.182

10.  1992 American Society of Human Genetics presidential address: back to the future.

Authors:  W E Nance
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

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