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A M Payne

Showing results (11-20 of 37) with videos related to

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European Journal of Human Genetics : EJHG|October 20, 2000
NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophiesD A Bessant, A M Payne, C Plant, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 19, 2000
Familial cavernous hemangioma: An expanding ocular spectrumD Sarraf, A M Payne, N D Kitchen, et al.
Human Heredity|March 17, 1999
Molecular genetic study of autosomal dominant retinitis pigmentosa in Lithuanian patientsV Kucinskas, A M Payne, D Ambrasiene, et al.
American Journal of Human Genetics|July 27, 1999
Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani originS Khaliq, A Hameed, M Ismail, et al.
Human Mutation|April 3, 1999
Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. OnlineD A Bessant, S Khaliq, A Hameed, et al.
American Journal of Human Genetics|May 23, 1998
A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32D A Bessant, S Khaliq, A Hameed, et al.
Investigative Ophthalmology & Visual Science|August 31, 2001
Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreousS Khaliq, A Hameed, M Ismail, et al.
Molecular Cell|August 14, 1998
GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophyI Sokal, N Li, I Surgucheva, et al.
Journal of Medical Genetics|October 3, 1999
Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophiesA M Payne, S M Downes, D A Bessant, et al.
Investigative Ophthalmology & Visual Science|May 31, 2001
A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani familyA Hameed, S Khaliq, M Ismail, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
European Journal of Human Genetics : EJHG|October 20, 2000
NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophiesD A Bessant, A M Payne, C Plant, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 19, 2000
Familial cavernous hemangioma: An expanding ocular spectrumD Sarraf, A M Payne, N D Kitchen, et al.
Human Heredity|March 17, 1999
Molecular genetic study of autosomal dominant retinitis pigmentosa in Lithuanian patientsV Kucinskas, A M Payne, D Ambrasiene, et al.
American Journal of Human Genetics|July 27, 1999
Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani originS Khaliq, A Hameed, M Ismail, et al.
Human Mutation|April 3, 1999
Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. OnlineD A Bessant, S Khaliq, A Hameed, et al.
American Journal of Human Genetics|May 23, 1998
A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32D A Bessant, S Khaliq, A Hameed, et al.
Investigative Ophthalmology & Visual Science|August 31, 2001
Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreousS Khaliq, A Hameed, M Ismail, et al.
Molecular Cell|August 14, 1998
GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophyI Sokal, N Li, I Surgucheva, et al.
Journal of Medical Genetics|October 3, 1999
Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophiesA M Payne, S M Downes, D A Bessant, et al.
Investigative Ophthalmology & Visual Science|May 31, 2001
A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani familyA Hameed, S Khaliq, M Ismail, et al.
Pageof 4