TYPICAL AND ATYPICAL MONOCHROMACY STUDIED BY SPECIFIC QUANTITATIVE PERIMETRY

Author:

HANSEN EGILL

Publisher

Wiley

Subject

Ophthalmology,General Medicine

Reference16 articles.

1. π1 cone monochromatism;Alpern;Arch. Ophthal. (Chicago),1965

2. Colour vision in bluecone “monochromacy”;Alpern;J. Physiol. (Lond.),1971

3. What is it that confines in a world without color;Alpern;Invest. Ophthal.,1974

4. Blue mono-cone monochromacy: A new color vision defect (Abstract);Blackwell;J. opt. Soc. Amer.,1957

5. Rod and cone receptor mechanisms in typical and atypical congenital achromatopsia;Blackwell;Vision Res.,1961

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1. Hereditary Cone Dystrophies;Albert &amp Jakobiec's Principles &amp Practice of Ophthalmology;2008

2. CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders;The American Journal of Human Genetics;2001-10

3. The cone dystrophies;Eye;1998-05

4. Loss of Inhibitory Mechanisms as a Measure of Cone Impairment: A Method Applied in Static Colour Perimetry;Documenta Ophthalmologica Proceedings Series;1983

5. A case of incomplete achromatopsia of the deutan type;Documenta Ophthalmologica;1981-11

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