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A M Payne

Showing results (21-30 of 37) with videos related to

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Veterinary Immunology and Immunopathology|December 11, 2007
Coccidia-induced mucogenesis promotes the onset of necrotic enteritis by supporting Clostridium perfringens growthC T Collier, C L Hofacre, A M Payne, et al.
The British Journal of Ophthalmology|July 22, 1999
Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32D A Bessant, K Anwar, S Khaliq, et al.
Investigative Ophthalmology & Visual Science|October 29, 2000
Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24S Khaliq, A Hameed, M Ismail, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 26, 1999
Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 familiesS M Downes, F W Fitzke, G E Holder, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 7, 2001
Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1S M Downes, G E Holder, F W Fitzke, et al.
Investigative Ophthalmology & Visual Science|March 11, 2000
A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13A Hameed, S Khaliq, M Ismail, et al.
Human Molecular Genetics|March 21, 1998
A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1A M Payne, S M Downes, D A Bessant, et al.
Journal of Medical Genetics|July 25, 2000
Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r)D A Bessant, A M Payne, B E Snow, et al.
Journal of Medical Genetics|September 22, 2001
Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophiesA M Payne, A G Morris, S M Downes, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

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Pageof 4
Veterinary Immunology and Immunopathology|December 11, 2007
Coccidia-induced mucogenesis promotes the onset of necrotic enteritis by supporting Clostridium perfringens growthC T Collier, C L Hofacre, A M Payne, et al.
The British Journal of Ophthalmology|July 22, 1999
Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32D A Bessant, K Anwar, S Khaliq, et al.
Investigative Ophthalmology & Visual Science|October 29, 2000
Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24S Khaliq, A Hameed, M Ismail, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 26, 1999
Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 familiesS M Downes, F W Fitzke, G E Holder, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 7, 2001
Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1S M Downes, G E Holder, F W Fitzke, et al.
Investigative Ophthalmology & Visual Science|March 11, 2000
A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13A Hameed, S Khaliq, M Ismail, et al.
Human Molecular Genetics|March 21, 1998
A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1A M Payne, S M Downes, D A Bessant, et al.
Journal of Medical Genetics|July 25, 2000
Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r)D A Bessant, A M Payne, B E Snow, et al.
Journal of Medical Genetics|September 22, 2001
Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophiesA M Payne, A G Morris, S M Downes, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.
Pageof 4