Literature DB >> 14203337

A HUE DISCRIMINATION DEFECT IN SO-CALLED NORMAL CARRIERS OF COLOR VISION DEFECTS.

A E KRILL, A SCHNEIDERMAN.   

Abstract

Keywords:  ADOLESCENCE; CHILD; COLOR BLINDNESS; COLOR PERCEPTION TESTS; GENES; GENETICS, HUMAN; SEX CHROMATIN

Mesh:

Year:  1964        PMID: 14203337

Source DB:  PubMed          Journal:  Invest Ophthalmol        ISSN: 0020-9988


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  3 in total

1.  On the incidence of unilateral and bilateral colour blindness in heterozygous females.

Authors:  K Feig; H H Ropers
Journal:  Hum Genet       Date:  1978-04-24       Impact factor: 4.132

2.  Color vision in albino subjects.

Authors:  P E Lourenço; G A FIshman; R J Anderson
Journal:  Doc Ophthalmol       Date:  1983-09-30       Impact factor: 2.379

3.  X-chromosomal-linked diseases affecting the eye: status of the heterozygote female.

Authors:  A E Krill
Journal:  Trans Am Ophthalmol Soc       Date:  1969
  3 in total

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