Distance and Sequence of the Loci for Protan and Deutan Defects and for Glucose-6-Phosphate Dehydrogenase Deficiency

PROOF for the separate localization on the human X -chromosome of the protanopia-protanomaly alleles and of the deuteranopia-deuteranomaly alleles requires the demonstration of: (1) non-allelic compound hemizygous males which in conditions of equilibrium should occur once among a thousand men (one i...

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Bibliographic Details
Published in:Nature (London) 1962-04, Vol.194 (4824), p.215-215
Main Author: KALMUS, H
Format: Article
Language:English
Subjects:
Color Vision Defects
Genetics, Medical
Glucosephosphate Dehydrogenase Deficiency
Humanities and Social Sciences
Humans
letter
Metabolic Diseases
multidisciplinary
Old Medline
Oxidoreductases - deficiency
Science
Science (multidisciplinary)
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Summary:PROOF for the separate localization on the human X -chromosome of the protanopia-protanomaly alleles and of the deuteranopia-deuteranomaly alleles requires the demonstration of: (1) non-allelic compound hemizygous males which in conditions of equilibrium should occur once among a thousand men (one in eighty colour-blind men) or of (2) crossover males in families combining both classes of defect.
ISSN:0028-0836
1476-4687
DOI:10.1038/194215a0