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	41.	Spectrum of mutations in USH2A in British patients with Usher syndrome type II. [electronic resource] by Leroy, B P Aragon-Martin, J A Weston, M D Bessant, D A Willis, C Webster, A R Bird, A C Kimberling, W J Payne, A M Bhattacharya, S S Producer: 20010607 In: Experimental eye research vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene. [electronic resource] by Dandekar, S S Ebenezer, N D Grayson, C Chapple, J P Egan, C A Holder, G E Jenkins, S A Fitzke, F W Cheetham, M E Webster, A R Hardcastle, A J Producer: 20040511 In: The British journal of ophthalmology vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract. [electronic resource] by Arora, A Minogue, P J Liu, X Reddy, M A Ainsworth, J R Bhattacharya, S S Webster, A R Hunt, D M Ebihara, L Moore, A T Beyer, E C Berthoud, V M Producer: 20061215 In: Journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections. [electronic resource] by Zito, I Downes, S M Patel, R J Cheetham, M E Ebenezer, N D Jenkins, S A Bhattacharya, S S Webster, A R Holder, G E Bird, A C Bamiou, D E Hardcastle, A J Producer: 20031103 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	An analysis of allelic variation in the ABCA4 gene. [electronic resource] by Webster, A R Héon, E Lotery, A J Vandenburgh, K Casavant, T L Oh, K T Beck, G Fishman, G A Lam, B L Levin, A Heckenlively, J R Jacobson, S G Weleber, R G Sheffield, V C Stone, E M Producer: 20010510 In: Investigative ophthalmology & visual science vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	46.	Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan. [electronic resource] by Zbar, B Kishida, T Chen, F Schmidt, L Maher, E R Richards, F M Crossey, P A Webster, A R Affara, N A Ferguson-Smith, M A Brauch, H Glavac, D Neumann, H P Tisherman, S Mulvihill, J J Gross, D J Shuin, T Whaley, J Seizinger, B Kley, N Olschwang, S Boisson, C Richard, S Lips, C H Lerman, M Producer: 19970328 In: Human mutation vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)