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Links from PubMed

Items: 8

1.

Color-deficient cone mosaics associated with Xq28 opsin mutations: a stop codon versus gene deletions.

Wagner-Schuman M, Neitz J, Rha J, Williams DR, Neitz M, Carroll J.

Vision Res. 2010 Nov 23;50(23):2396-402. doi: 10.1016/j.visres.2010.09.015. Epub 2010 Sep 17.

2.

Molecular genetics of color-vision deficiencies.

Deeb SS.

Vis Neurosci. 2004 May-Jun;21(3):191-6. Review.

PMID:
15518188
3.

[Inherited colour vision deficiencies--from Dalton to molecular genetics].

Cvetković D, Cvetković D.

Srp Arh Celok Lek. 2005 Nov-Dec;133(11-12):521-7. Review. Serbian.

4.

Genetics of color vision deficiencies.

Deeb SS, Kohl S.

Dev Ophthalmol. 2003;37:170-87. Review.

PMID:
12876837
5.

Genetics of variation in human color vision and the retinal cone mosaic.

Deeb SS.

Curr Opin Genet Dev. 2006 Jun;16(3):301-7. Epub 2006 May 2. Review.

PMID:
16647849
6.

The molecular basis of variation in human color vision.

Deeb SS.

Clin Genet. 2005 May;67(5):369-77. Review.

PMID:
15811001
7.

The genetics of normal and defective color vision.

Neitz J, Neitz M.

Vision Res. 2011 Apr 13;51(7):633-51. doi: 10.1016/j.visres.2010.12.002. Epub 2010 Dec 15. Review.

8.

A perspective on color vision in platyrrhine monkeys.

Jacobs GH.

Vision Res. 1998 Nov;38(21):3307-13. Review.

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