PubMed (OMIM) for id: 2652

Year	Number of Results
1954	1
1960	1
1962	2
1964	1
1965	1
1968	1
1970	1
1972	1
1973	1
1974	1
1977	2
1978	1
1982	1
1984	1
1986	4
1987	3
1988	1
1989	2
1991	2
1992	4
1993	1
1994	1
1995	3
1996	2
1997	1
1999	2
2000	1
2001	2
2002	2
2003	1
2005	2
2009	1
2010	1
2024	0

1

X-linked cone dystrophy caused by mutation of the red and green cone opsins.

Gardner JC, Webb TR, Kanuga N, Robson AG, Holder GE, Stockman A, Ripamonti C, Ebenezer ND, Ogun O, Devery S, Wright GA, Maher ER, Cheetham ME, Moore AT, Michaelides M, Hardcastle AJ. Gardner JC, et al. Am J Hum Genet. 2010 Jul 9;87(1):26-39. doi: 10.1016/j.ajhg.2010.05.019. Epub 2010 Jun 24. Am J Hum Genet. 2010. PMID: 20579627 Free PMC article.

2

Blue cone monochromacy: causative mutations and associated phenotypes.

Gardner JC, Michaelides M, Holder GE, Kanuga N, Webb TR, Mollon JD, Moore AT, Hardcastle AJ. Gardner JC, et al. Mol Vis. 2009;15:876-84. Epub 2009 May 1. Mol Vis. 2009. PMID: 19421413 Free PMC article.

3

The molecular basis of variation in human color vision.

Deeb SS. Deeb SS. Clin Genet. 2005 May;67(5):369-77. doi: 10.1111/j.1399-0004.2004.00343.x. Clin Genet. 2005. PMID: 15811001 Review.

4

Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals.

Michaelides M, Johnson S, Simunovic MP, Bradshaw K, Holder G, Mollon JD, Moore AT, Hunt DM. Michaelides M, et al. Eye (Lond). 2005 Jan;19(1):2-10. doi: 10.1038/sj.eye.6701391. Eye (Lond). 2005. PMID: 15094734

5

Linkage between glucose-6-phosphate dehydrogenase deficiency and colour-blindness.

PORTER IH, SCHULZE J, McKUSICK VA. PORTER IH, et al. Nature. 1962 Feb 3;193:506. doi: 10.1038/193506a0. Nature. 1962. PMID: 14488077 No abstract available.

6

THE X-LINKED RECESSIVE INHERITANCE OF ATYPICAL MONOCHROMATISM.

SPIVEY BE. SPIVEY BE. Arch Ophthalmol. 1965 Sep;74:327-33. doi: 10.1001/archopht.1965.00970040329007. Arch Ophthalmol. 1965. PMID: 14338644 No abstract available.

7

RECOMBINATION BETWEEN PROTAN AND DEUTAN GENES; DATA ON THEIR RELATIVE POSITONS IN RESPECT OF THE G6PD LOCUS.

SINISCALCO M, FILIPPI G, LATTE B. SINISCALCO M, et al. Nature. 1964 Dec 12;204:1062-4. doi: 10.1038/2041062a0. Nature. 1964. PMID: 14243382 No abstract available.

8

Genetical linkage between the loci for glucose-6-phosphate dehydrogenase deficiency and colour-blindness in American Negroes.

PORTER IH, SCHULZE J, MCKUSICK VA. PORTER IH, et al. Ann Hum Genet. 1962 Nov;26:107-22. doi: 10.1111/j.1469-1809.1962.tb01316.x. Ann Hum Genet. 1962. PMID: 13985567 No abstract available.

9

The enigma of typical total monochromacy.

ALPERN M, FALLS HF, LEE GB. ALPERN M, et al. Am J Ophthalmol. 1960 Nov;50:996-1012. doi: 10.1016/0002-9394(60)90353-6. Am J Ophthalmol. 1960. PMID: 13682677 No abstract available.

10

Congenital achromatopsia; a report of 19 cases.

SLOAN LL. SLOAN LL. J Opt Soc Am. 1954 Feb;44(2):117-28. doi: 10.1364/josa.44.000117. J Opt Soc Am. 1954. PMID: 13131176 No abstract available.

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