Genotype-phenotype relationships in human red/green color-vision defects: Molecular and psychophysical studies

American Journal of Human Genetics

Volumn 51, Issue 4, 1992, Pages 687-700

  Deeb, S S ^a   Lindsey, D T ^a   Hibiya, Y ^a   Sanocki, E ^a   Winderickx, J ^a   Teller, D Y ^a   Motulsky, A G ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

VISUAL PIGMENT;

ARTICLE; CAUCASIAN; COLOR VISION DEFECT; COLOR VISION TEST; DNA SEQUENCE; EXON; GENE DELETION; GENOTYPE; HETEROZYGOTE; HUMAN; HYBRID GENE; INTRON; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PSYCHOPHYSIOLOGY; X CHROMOSOME LINKAGE;

BASE SEQUENCE; BLOTTING, SOUTHERN; CAUCASOID RACE; COLOR PERCEPTION; COLOR VISION DEFECTS; DNA; GENOTYPE; HUMAN; LEUKOCYTES; MALE; MOLECULAR SEQUENCE DATA; NEGROID RACE; OLIGODEOXYRIBONUCLEOTIDES; PHENOTYPE; POLYMERASE CHAIN REACTION; RESTRICTION MAPPING; RETINAL PIGMENTS; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0026661795     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)