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	1.	Lamellar keratoplasty in the management of inflammatory corneal ulceration and perforation. [electronic resource] by Bessant, D A Dart, J K Producer: 19940728 In: Eye (London, England) vol. 8 ( Pt 1) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Management of strabismus due to orbital myositis. [electronic resource] by Bessant, D A Lee, J P Producer: 19960213 In: Eye (London, England) vol. 9 ( Pt 5) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Molecular genetics and prospects for therapy of the inherited retinal dystrophies. [electronic resource] by Bessant, D A Ali, R R Bhattacharya, S S Producer: 20011101 In: Current opinion in genetics & development vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The management of dislocated lens material after phacoemulsification. [electronic resource] by Bessant, D A Sullivan, P M Aylward, G W Producer: 19981217 In: Eye (London, England) vol. 12 ( Pt 4) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Results of excimer laser retreatment of residual myopia after previous photorefractive keratectomy. [electronic resource] by Chatterjee, A Shah, S Bessant, D A Doyle, S J Producer: 19970911 In: Ophthalmology vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Epithelial debridement for secondary hyperopia following myopic excimer laser photorefractive keratectomy. [electronic resource] by Shah, S Chatterjee, A Doyle, S J Bessant, D A Producer: 19980326 In: Journal of cataract and refractive surgery vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Astigmatism induced by spherical photorefractive keratectomy corrections. [electronic resource] by Shah, S Chatterjee, A Doyle, S J Bessant, D A Producer: 19970911 In: Ophthalmology vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Reduction in intraocular pressure after excimer laser photorefractive keratectomy. Correlation with pretreatment myopia. [electronic resource] by Chatterjee, A Shah, S Bessant, D A Naroo, S A Doyle, S J Producer: 19970401 In: Ophthalmology vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Further refinement of the Usher 2A locus at 1q41. [electronic resource] by Bessant, D A Payne, A M Plant, C Bird, A C Bhattacharya, S S Producer: 19981110 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Founder effect, seen in the British population, of the 172 peripherin/RDS mutation-and further refinement of genetic positioning of the peripherin/RDS gene. [electronic resource] by Payne, A M Downes, S M Bessant, D A Bird, A C Bhattacharya, S S Producer: 19980304 In: American journal of human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies. [electronic resource] by Bessant, D A Payne, A M Plant, C Bird, A C Swaroop, A Bhattacharya, S S Producer: 20010201 In: European journal of human genetics : EJHG vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin. [electronic resource] by Khaliq, S Hameed, A Ismail, M Mehdi, S Q Bessant, D A Payne, A M Bhattacharya, S S Producer: 19990820 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32. [electronic resource] by Bessant, D A Khaliq, S Hameed, A Anwar, K Mehdi, S Q Payne, A M Bhattacharya, S S Producer: 19980521 In: American journal of human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. Online. [electronic resource] by Bessant, D A Khaliq, S Hameed, A Anwar, K Payne, A M Mehdi, S Q Bhattacharya, S S Producer: 19990401 In: Human mutation vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies. [electronic resource] by Payne, A M Downes, S M Bessant, D A Plant, C Moore, T Bird, A C Bhattacharya, S S Producer: 19991027 In: Journal of medical genetics vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	16.	Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32. [electronic resource] by Bessant, D A Anwar, K Khaliq, S Hameed, A Ismail, M Payne, A M Mehdi, S Q Bhattacharya, S S Producer: 20000111 In: The British journal of ophthalmology vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 families. [electronic resource] by Downes, S M Fitzke, F W Holder, G E Payne, A M Bessant, D A Bhattacharya, S S Bird, A C Producer: 19991027 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1. [electronic resource] by Payne, A M Downes, S M Bessant, D A Taylor, R Holder, G E Warren, M J Bird, A C Bhattacharya, S S Producer: 19980317 In: Human molecular genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r) [electronic resource] by Bessant, D A Payne, A M Snow, B E Antiño, G Mehdi, S Q Bird, A C Siderovski, D P Bhattacharya, S S Producer: 20000717 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	A mutation in NRL is associated with autosomal dominant retinitis pigmentosa. [electronic resource] by Bessant, D A Payne, A M Mitton, K P Wang, Q L Swain, P K Plant, C Bird, A C Zack, D J Swaroop, A Bhattacharya, S S Producer: 19990426 In: Nature genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 21 results.