D F Roberts|S S Papiha|S S Bhattacharya - JoVE Visualize

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Genomics|September 1, 1991

Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment siteT J Keen, C F Inglehearn, D H Lester, et al.

Annals of Human Genetics|September 7, 2007

Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRsI Barragán, S Borrego, M M Abd El-Aziz, et al.

Human Molecular Genetics|September 26, 2000

Functional impairment of lens aquaporin in two families with dominantly inherited cataractsP Francis, J J Chung, M Yasui, 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.

Environmental Pollution (Barking, Essex : 1987)|November 22, 2015

The effects of composting approaches on the emissions of anthropogenic volatile organic compounds: A comparison between vermicomposting and general aerobic compostingS S Bhattacharya, Ki-Hyun Kim, Md Ahsan Ullah, et al.

Eye (London, England)|March 16, 2004

BIGH3 mutation in a Bangladeshi family with a variable phenotype of LCDIM F El-Ashry, M M Abd El-Aziz, L A Ficker, et al.

Molecular Vision|August 4, 2006

A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic familyP K F Addison, V Berry, K R Holden, 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.

Clinical Endocrinology|February 1, 1980

HLA antigens and thyroid autoantibodies in patients with Graves' disease and their first degree relativesB A Mather, D F Roberts, M F Scanlon, et al.

Journal of Medical Genetics|February 25, 1998

A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneityC F Inglehearn, E E Tarttelin, C Plant, et al.

Pageof 37

Showing results (291-300 of 365) with videos related to

Sort By:

Pageof 37

Genomics|September 1, 1991

Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment siteT J Keen, C F Inglehearn, D H Lester, et al.

Annals of Human Genetics|September 7, 2007

Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRsI Barragán, S Borrego, M M Abd El-Aziz, et al.

Human Molecular Genetics|September 26, 2000

Functional impairment of lens aquaporin in two families with dominantly inherited cataractsP Francis, J J Chung, M Yasui, 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.

Environmental Pollution (Barking, Essex : 1987)|November 22, 2015

The effects of composting approaches on the emissions of anthropogenic volatile organic compounds: A comparison between vermicomposting and general aerobic compostingS S Bhattacharya, Ki-Hyun Kim, Md Ahsan Ullah, et al.

Eye (London, England)|March 16, 2004

BIGH3 mutation in a Bangladeshi family with a variable phenotype of LCDIM F El-Ashry, M M Abd El-Aziz, L A Ficker, et al.

Molecular Vision|August 4, 2006

A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic familyP K F Addison, V Berry, K R Holden, 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.

Clinical Endocrinology|February 1, 1980

HLA antigens and thyroid autoantibodies in patients with Graves' disease and their first degree relativesB A Mather, D F Roberts, M F Scanlon, et al.

Journal of Medical Genetics|February 25, 1998

A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneityC F Inglehearn, E E Tarttelin, C Plant, et al.

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