Literature DB >> 13238560

A sign of manifest heterozygosity in carriers of color deficiency.

I SCHMIDT.   

Abstract

Entities:  

Keywords:  COLOR VISION

Mesh：

Year:  1955        PMID： 13238560     DOI： 10.1097/00006324-195508000-00003

Source DB:  PubMed          Journal:  Am J Optom Arch Am Acad Optom        ISSN： 0002-9408


× No keyword cloud information.
  4 in total

1.  Electroretinogram analysis of relative spectral sensitivity in genetically identified dichromatic macaques.

Authors:  A Hanazawa; A Mikami; P Sulistyo Angelika; O Takenaka; S Goto; A Onishi; S Koike; T Yamamori; K Kato; A Kondo; B Suryobroto; A Farajallah; H Komatsu
Journal:  Proc Natl Acad Sci U S A       Date:  2001-06-26       Impact factor: 11.205

2.  [Chromosomal anomalies and the heredity of acquired color sense disorders].

Authors:  R G FREY
Journal:  Albrecht Von Graefes Arch Ophthalmol       Date:  1961

3.  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

4.  Richer color experience in observers with multiple photopigment opsin genes.

Authors:  K A Jameson; S M Highnote; L M Wasserman
Journal:  Psychon Bull Rev       Date:  2001-06
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.