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	1.	Identification and characterization of C6orf37, a novel candidate human retinal disease gene on chromosome 6q14. [electronic resource] by Lagali, P S Kakuk, L E Griesinger, I B Wong, P W Ayyagari, R Producer: 20020705 In: Biochemical and biophysical research communications vol. 293 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment gene. [electronic resource] by Ayyagari, R Kakuk, L E Coats, C L Bingham, E L Toda, Y Felius, J Sieving, P A Producer: 19990805 In: Molecular vision vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	3.	Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy. [electronic resource] by Ayyagari, R Kakuk, L E Bingham, E L Szczesny, J J Kemp, J Toda, Y Felius, J Sieving, P A Producer: 20000921 In: Human genetics vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Bestrophin gene mutations in patients with Best vitelliform macular dystrophy. [electronic resource] by Caldwell, G M Kakuk, L E Griesinger, I B Simpson, S A Nowak, N J Small, K W Maumenee, I H Rosenfeld, P J Sieving, P A Shows, T B Ayyagari, R Producer: 19990706 In: Genomics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Evaluation of the ELOVL4 gene in patients with age-related macular degeneration. [electronic resource] by Ayyagari, R Zhang, K Hutchinson, A Yu, Z Swaroop, A Kakuk, L E Seddon, J M Bernstein, P S Lewis, R A Tammur, J Yang, Z Li, Y Zhang, H Yashar, B M Liu, J Petrukhin, K Sieving, P A Allikmets, R Producer: 20020208 In: Ophthalmic genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy. [electronic resource] by Zhang, K Kniazeva, M Han, M Li, W Yu, Z Yang, Z Li, Y Metzker, M L Allikmets, R Zack, D J Kakuk, L E Lagali, P S Wong, P W MacDonald, I M Sieving, P A Figueroa, D J Austin, C P Gould, R J Ayyagari, R Petrukhin, K Producer: 20010201 In: Nature genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)