These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
178 related articles for article (PubMed ID: 8739504)
1. Detection of congenital color vision defects using heteroduplex-SSCP analysis. Zhang Q; Minoda K Jpn J Ophthalmol; 1996; 40(1):79-85. PubMed ID: 8739504 [TBL] [Abstract][Full Text] [Related]
2. [Analysis of fusion points in hybrid genes and gene deletion for congenital red-green color vision defects]. Shen H; Zhang Q; Xiao X; Li S; Guo L; Jiang F Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):290-2. PubMed ID: 10514533 [TBL] [Abstract][Full Text] [Related]
3. Molecular basis of congenital color vision defects in Chinese patients. Zhang Q; Mao W; Ma Q; Zeng R; Wu L; Wu DZ; Chen Y Jpn J Ophthalmol; 1992; 36(4):479-87. PubMed ID: 1289623 [TBL] [Abstract][Full Text] [Related]
4. Color vision defects with variation in the exon 5 of red and green pigment genes. Shen H; Zhang Q; Xiao X; Li S; Guo L; Jiang F Yan Ke Xue Bao; 1998 Sep; 14(3):130-3. PubMed ID: 12580020 [TBL] [Abstract][Full Text] [Related]
5. [A comparative study of the detection of abnormal visual pigment genes by PCR and hybridization]. Zhang QJ Zhonghua Yan Ke Za Zhi; 1993 Nov; 29(6):356-8. PubMed ID: 8020380 [TBL] [Abstract][Full Text] [Related]
6. Single 5'green-3'red hybrid gene in protanopia. Zhang Q; Minoda K Yan Ke Xue Bao; 1996 Mar; 12(1):5-9. PubMed ID: 9275729 [TBL] [Abstract][Full Text] [Related]
7. Analysis of L-cone/M-cone visual pigment gene arrays in Japanese males with protan color-vision deficiency. Ueyama H; Kuwayama S; Imai H; Oda S; Nishida Y; Tanabe S; Shichida Y; Yamade S Vision Res; 2004; 44(19):2241-52. PubMed ID: 15208011 [TBL] [Abstract][Full Text] [Related]
8. The molecular basis of variation in human color vision. Deeb SS Clin Genet; 2005 May; 67(5):369-77. PubMed ID: 15811001 [TBL] [Abstract][Full Text] [Related]
9. Number and variations of the red and green visual pigment genes in Japanese men with normal color vision. Hayashi S; Ueyama H; Tanabe S; Yamade S; Kani K Jpn J Ophthalmol; 2001; 45(1):60-7. PubMed ID: 11163047 [TBL] [Abstract][Full Text] [Related]
10. Detection of female carriers of congenital color-vision deficiencies by visual pigment gene analysis. Oda S; Ueyama H; Tanabe S; Tanaka Y; Yamade S; Kani K Curr Eye Res; 2000 Oct; 21(4):767-73. PubMed ID: 11120566 [TBL] [Abstract][Full Text] [Related]
11. Genotype-phenotype relationships in human red/green color-vision defects: molecular and psychophysical studies. Deeb SS; Lindsey DT; Hibiya Y; Sanocki E; Winderickx J; Teller DY; Motulsky AG Am J Hum Genet; 1992 Oct; 51(4):687-700. PubMed ID: 1415215 [TBL] [Abstract][Full Text] [Related]
12. Direct genomic multiplex PCR for BRCA1 and application to mutation detection by single-strand conformation and heteroduplex analysis. Barker DF Hum Mutat; 2000 Oct; 16(4):334-44. PubMed ID: 11013444 [TBL] [Abstract][Full Text] [Related]
13. Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype. Hayashi T; Motulsky AG; Deeb SS Nat Genet; 1999 May; 22(1):90-3. PubMed ID: 10319869 [TBL] [Abstract][Full Text] [Related]
14. Polymorphism in the number of genes encoding long-wavelength-sensitive cone pigments among males with normal color vision. Neitz M; Neitz J; Grishok A Vision Res; 1995 Sep; 35(17):2395-407. PubMed ID: 8594809 [TBL] [Abstract][Full Text] [Related]
15. Analysis of fusion gene and encoded photopigment of colour-blind humans. Neitz J; Neitz M; Jacobs GH Nature; 1989 Dec; 342(6250):679-82. PubMed ID: 2574415 [TBL] [Abstract][Full Text] [Related]
16. Novel form of a single X-linked visual pigment gene in a unique dichromatic color-vision defect. Hayashi T; Kubo A; Takeuchi T; Gekka T; Goto-Omoto S; Kitahara K Vis Neurosci; 2006; 23(3-4):411-7. PubMed ID: 16961974 [TBL] [Abstract][Full Text] [Related]
17. [Visual pigment genes for color vision defects]. Zhang Q; Mao W; Ma Q; Zeng R; Wu L; Wu D; Chen Y Yan Ke Xue Bao; 1990 Dec; 6(3-4):51-7. PubMed ID: 2101366 [TBL] [Abstract][Full Text] [Related]
18. The most frequent APC mutations among Slovak familial adenomatous polyposis patients. Adenomatous polyposis coli. Zajac V; Kovác M; Kirchhoff T; Stevurková V; Tomka M Neoplasma; 2002; 49(6):356-61. PubMed ID: 12584582 [TBL] [Abstract][Full Text] [Related]