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Results: 1 to 20 of 38

1.

X-linked high myopia associated with cone dysfunction.

Young TL, Deeb SS, Ronan SM, Dewan AT, Alvear AB, Scavello GS, Paluru PC, Brott MS, Hayashi T, Holleschau AM, Benegas N, Schwartz M, Atwood LD, Oetting WS, Rosenberg T, Motulsky AG, King RA.

Arch Ophthalmol. 2004 Jun;122(6):897-908.

PMID:
15197065
[PubMed - indexed for MEDLINE]
2.

Genetics of color vision deficiencies.

Deeb SS, Kohl S.

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

PMID:
12876837
[PubMed - indexed for MEDLINE]
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.

PMID:
16758855
[PubMed - indexed for MEDLINE]
4.

[Genetics of congenital color vision defects. II. Rare types of color blindness].

Krawczyński MR.

Klin Oczna. 1995 Jan-Feb;97(1-2):39-43. Review. Polish.

PMID:
7637312
[PubMed - indexed for MEDLINE]
5.

[Molecular genetics of red-green color blindness].

Ladekjaer-Mikkelsen AS, Jensen H, Rosenberg T, Jørgensen AL.

Ugeskr Laeger. 1995 Aug 28;157(35):4808-12. Review. Danish.

PMID:
7676516
[PubMed - indexed for MEDLINE]
6.

The molecular genetics and evolution of primate colour vision.

Tovee MJ.

Trends Neurosci. 1994 Jan;17(1):30-7. Review.

PMID:
7511848
[PubMed - indexed for MEDLINE]
7.

X-linked recessive inheritance of radial ray deficiencies in a family with four affected males.

Galjaard RJ, Kostakoglu N, Hoogeboom JJ, Breedveld GJ, van der Linde HC, Hovius SE, Oostra BA, Sandkuijl LA, Akarsu AN, Heutink P.

Eur J Hum Genet. 2001 Sep;9(9):653-8. Review.

PMID:
11571552
[PubMed - indexed for MEDLINE]
Free Article
8.

[Genetics of congenital color vision defects. I. Common types of color blindness].

Krawczyński MR.

Klin Oczna. 1995 Jan-Feb;97(1-2):34-8. Review. Polish.

PMID:
7637311
[PubMed - indexed for MEDLINE]
9.

Molecular genetics of color-vision deficiencies.

Deeb SS.

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

PMID:
15518188
[PubMed - indexed for MEDLINE]
10.

The molecular genetics of color vision and color blindness.

Piantanida T.

Trends Genet. 1988 Nov;4(11):319-23. Review. No abstract available.

PMID:
2907192
[PubMed - indexed for MEDLINE]
11.

[Progressive cone dystrophy: electrophysiological changes in female carriers].

Amzallag T, Puech B, Hache JC, François P.

J Fr Ophtalmol. 1990;13(8-9):421-8. Review. French.

PMID:
2081853
[PubMed - indexed for MEDLINE]
12.

A perspective on color vision in platyrrhine monkeys.

Jacobs GH.

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

PMID:
9893842
[PubMed - indexed for MEDLINE]
Free Article
13.

Molecular genetics of human color vision.

Deeb SS, Motulsky AG.

Behav Genet. 1996 May;26(3):195-207. Review.

PMID:
8754247
[PubMed - indexed for MEDLINE]
14.

Manifestations in four males with and an obligate carrier of the Lenz microphthalmia syndrome.

Forrester S, Kovach MJ, Reynolds NM, Urban R, Kimonis V.

Am J Med Genet. 2001 Jan 1;98(1):92-100. Review.

PMID:
11426460
[PubMed - indexed for MEDLINE]
15.

Recent gene conversion between genes encoding human red and green visual pigments.

Kuma K, Hayashida H, Miyata T.

Jpn J Genet. 1988 Aug;63(4):367-71. Review.

PMID:
3078877
[PubMed - indexed for MEDLINE]
Free Article
16.

Colour vision. Dalton's eyes and monkey genes.

Tovée MJ.

Curr Biol. 1995 Jun 1;5(6):583-6. Review.

PMID:
7552161
[PubMed - indexed for MEDLINE]
Free Article
17.

X-linked dominant control of F-cells in normal adult life: characterization of the Swiss type as hereditary persistence of fetal hemoglobin regulated dominantly by gene(s) on X chromosome.

Miyoshi K, Kaneto Y, Kawai H, Ohchi H, Niki S, Hasegawa K, Shirakami A, Yamano T.

Blood. 1988 Dec;72(6):1854-60. Review.

PMID:
2461753
[PubMed - indexed for MEDLINE]
Free Article
18.

X-linked congenital stationary night blindness. Review and report of a family with hyperopia.

Khouri G, Mets MB, Smith VC, Wendell M, Pass AS.

Arch Ophthalmol. 1988 Oct;106(10):1417-22. Review.

PMID:
3052384
[PubMed - indexed for MEDLINE]
19.

[The molecular genetics of color blindness].

Miki N.

Nihon Ganka Gakkai Zasshi. 1991 Dec;95(12):1196-205. Review. Japanese.

PMID:
1776601
[PubMed - indexed for MEDLINE]
20.

[Molecular genetics of adrenoleukodystrophy].

Kaneko K.

Nihon Rinsho. 1993 Sep;51(9):2359-63. Review. Japanese.

PMID:
8411713
[PubMed - indexed for MEDLINE]

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