Your search returned 78 results.

Results
	61.	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)
	62.	Adenoviruses: group name proposed for new respiratory-tract viruses. [electronic resource] by ENDERS, J F BELL, J A DINGLE, J H FRANCIS, T HILLEMAN, M R HUEBNER, R J PAYNE, A M Producer: 20030501 In: Science (New York, N.Y.) vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	Coccidia-induced mucogenesis promotes the onset of necrotic enteritis by supporting Clostridium perfringens growth. [electronic resource] by Collier, C T Hofacre, C L Payne, A M Anderson, D B Kaiser, P Mackie, R I Gaskins, H R Producer: 20080422 In: Veterinary immunology and immunopathology vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24. [electronic resource] by Khaliq, S Hameed, A Ismail, M Anwar, K Leroy, B P Mehdi, S Q Payne, A M Bhattacharya, S S Producer: 20001114 In: Investigative ophthalmology & visual science vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	65.	Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1. [electronic resource] by Downes, S M Holder, G E Fitzke, F W Payne, A M Warren, M J Bhattacharya, S S Bird, A C Producer: 20010125 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 119 Availability: No items available. Save to lists Add to cart (remove)
	66.	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)
	67.	A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13. [electronic resource] by Hameed, A Khaliq, S Ismail, M Anwar, K Ebenezer, N D Jordan, T Mehdi, S Q Payne, A M Bhattacharya, S S Producer: 20000315 In: Investigative ophthalmology & visual science vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	68.	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)
	69.	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)
	70.	Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies. [electronic resource] by Payne, A M Morris, A G Downes, S M Johnson, S Bird, A C Moore, A T Bhattacharya, S S Hunt, D M Producer: 20020110 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1. [electronic resource] by Downes, S M Payne, A M Kelsell, R E Fitzke, F W Holder, G E Hunt, D M Moore, A T Bird, A C Producer: 20011228 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	72.	Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy. [electronic resource] by Kelsell, R E Gregory-Evans, K Payne, A M Perrault, I Kaplan, J Yang, R B Garbers, D L Bird, A C Moore, A T Hunt, D M Producer: 19990112 In: Human molecular genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	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)
	74.	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)
	75.	Prevalence of AIPL1 mutations in inherited retinal degenerative disease. [electronic resource] by Sohocki, M M Perrault, I Leroy, B P Payne, A M Dharmaraj, S Bhattacharya, S S Kaplan, J Maumenee, I H Koenekoop, R Meire, F M Birch, D G Heckenlively, J R Daiger, S P Producer: 20000822 In: Molecular genetics and metabolism vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	76.	Extragenic suppressors of the nimX2(cdc2) mutation of Aspergillus nidulans affect nuclear division, septation and conidiation. [electronic resource] by McGuire, S L Roe, D L Carter, B W Carter, R L Grace, S P Hays, P L Lang, G A Mamaril, J L McElvaine, A T Payne, A M Schrader, M D Wahrle, S E Young, C D Producer: 20010215 In: Genetics vol. 156 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	77.	Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. [electronic resource] by Sohocki, M M Bowne, S J Sullivan, L S Blackshaw, S Cepko, C L Payne, A M Bhattacharya, S S Khaliq, S Qasim Mehdi, S Birch, D G Harrison, W R Elder, F F Heckenlively, J R Daiger, S P Producer: 20000210 In: Nature genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	78.	Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12). [electronic resource] by den Hollander, A I ten Brink, J B de Kok, Y J van Soest, S van den Born, L I van Driel, M A van de Pol, D J Payne, A M Bhattacharya, S S Kellner, U Hoyng, C B Westerveld, A Brunner, H G Bleeker-Wagemakers, E M Deutman, A F Heckenlively, J R Cremers, F P Bergen, A A Producer: 19991019 In: Nature genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)