THE GENETICS OF ALCOHOLISM AND COLOR BLINDNESS.
- Published in:
- Nutrition Reviews, 1967, v. 25, n. 5, p. 138, doi. 10.1111/j.1753-4887.1967.tb05609.x
- Publication type:
- Article
Works matching Color blindness and genetics
Results: 16
1
2
Genetic studies in a family with testicular feminization, haemophilia A and colour blindness.
- Published in:
- Clinical Genetics, 1972, v. 3, n. 4, p. 253, doi. 10.1111/j.1399-0004.1972.tb04273.x
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- Publication type:
- Article
3
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.
- Published in:
- Nature, 1983, v. 306, n. 5944, p. 701, doi. 10.1038/306701a0
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- Publication type:
- Article
4
Prevalence of Colour Blindness in Young Jordanians.
- Published in:
- Ophthalmologica, 2001, v. 215, n. 1, p. 39, doi. 10.1159/000050824
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- Publication type:
- Article
5
Mutations in the CNGB3 gene encoding the β -subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3 ) linked to chromosome 8q21.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 14, p. 2107, doi. 10.1093/hmg/9.14.2107
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- Publication type:
- Article
6
Towards a Military Medical Ethics Framework for Genetic Human Enhancement.
- Published in:
- Penn Bioethics Journal, 2010, v. 6, n. 1, p. 8
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- Publication type:
- Article
7
CIRRHOSIS OF THE LIVER AND COLOR BLINDNESS.
- Published in:
- Nutrition Reviews, 1965, v. 23, n. 10, p. 293, doi. 10.1111/j.1753-4887.1965.tb02032.x
- Publication type:
- Article
8
A Population Genetic Study of the Vania Soni in Western India.
- Published in:
- Human Heredity, 1978, v. 28, n. 2, p. 104, doi. 10.1159/000152951
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- Publication type:
- Article
9
Some Genetic Interrelationships in England and Wales.
- Published in:
- Human Heredity, 1974, v. 24, n. 5/6, p. 540, doi. 10.1159/000152692
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- Publication type:
- Article
10
A new mutation in the PDE6C gene in achromatopsia.
- Published in:
- European Journal of Ophthalmology, 2023, v. 33, n. 4, p. NP133, doi. 10.1177/11206721221093023
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- Publication type:
- Article
11
Recent Advancements in Gene Therapy for Hereditary Retinal Dystrophies.
- Published in:
- Turkish Journal of Ophthalmology / Turk Oftalmoloji Dergisi, 2017, v. 47, n. 6, p. 338, doi. 10.4274/tjo.41017
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- Publication type:
- Article
12
Prevalence of Color Blindness in Iranian Students: A Meta-analysis.
- Published in:
- Journal of Ophthalmic & Vision Research, 2022, v. 17, n. 3, p. 413, doi. 10.18502/jovr.v17i3.11580
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- Publication type:
- Article
13
Dyschromatopsia: a comprehensive analysis of mechanisms and cutting-edge treatments for color vision deficiency.
- Published in:
- Frontiers in Neuroscience, 2024, p. 01, doi. 10.3389/fnins.2024.1265630
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- Publication type:
- Article
14
Confessions of a deuteranope.
- Published in:
- Europhysics News, 2016, v. 47, n. 5/6, p. 16, doi. 10.1051/epn/2016501
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- Publication type:
- Article
15
Gene therapy for red–green colour blindness in adult primates.
- Published in:
- Nature, 2009, v. 461, n. 7265, p. 784, doi. 10.1038/nature08401
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- Publication type:
- Article
16
Vision: Gene therapy in colour.
- Published in:
- Nature, 2009, v. 461, n. 7265, p. 737, doi. 10.1038/461737a
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- Publication type:
- Article