Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32
Bessant, David A R, Anwar, Khalid, Khaliq, Shagufta, Hameed, Abdul, Ismail, M, Payne, Annette M, Mehdi, S Qasim, Bhattacharya, Shomi S
Published in British journal of ophthalmology (01.08.1999)
Published in British journal of ophthalmology (01.08.1999)
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Journal Article
A Mutation in Guanylate Cyclase Activator 1A (GUCA1A) in an Autosomal Dominant Cone Dystrophy Pedigree Mapping to a New Locus on Chromosome 6p21.1
Payne, Annette M., Downes, Susan M., Bessant, David A.R., Taylor, Rachel, Holder, Graham E., Warren, Martin J., Bird, Alan C., Bhattacharya, Shomi S.
Published in Human molecular genetics (01.02.1998)
Published in Human molecular genetics (01.02.1998)
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Journal Article
A Locus for Autosomal Recessive Congenital Microphthalmia Maps to Chromosome 14q32
Bessant, David A.R., Khaliq, Shagufta, Hameed, Abdul, Anwar, Khalid, Mehdi, S. Qasim, Payne, Annette M., Bhattacharya, Shomi S.
Published in American journal of human genetics (01.05.1998)
Published in American journal of human genetics (01.05.1998)
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Journal Article
Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies
Payne, Annette M, Downes, Susan M, Bessant, David A R, Plant, Catherine, Moore, Tony, Bird, Alan C, Bhattacharya, Shomi S
Published in Journal of medical genetics (01.09.1999)
Published in Journal of medical genetics (01.09.1999)
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Journal Article
Astigmatism Induced by Spherical Photorefractive Keratectomy Corrections
Shah, Sunil, Chatterjee, Anupam, Doyle, Stephen J., Bessant, David A.R.
Published in Ophthalmology (Rochester, Minn.) (01.08.1997)
Published in Ophthalmology (Rochester, Minn.) (01.08.1997)
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Journal Article
Further refinement of the Usher 2A locus at 1q41
Bessant, D A, Payne, A M, Plant, C, Bird, A C, Bhattacharya, S S
Published in Journal of medical genetics (01.09.1998)
Published in Journal of medical genetics (01.09.1998)
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Journal Article
Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r)
BESSANT, DAVID A R, PAYNE, ANNETTE M, SNOW, BRYAN E, ANTIÑOLO, GUILLERMO, MEHDI, S QASIM, BIRD, ALAN C, SIDEROVSKI, DAVID P, BHATTACHARYA, SHOMI S
Published in Journal of medical genetics (01.05.2000)
Published in Journal of medical genetics (01.05.2000)
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Journal Article
Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 families
Downes, S M, Fitzke, F W, Holder, G E, Payne, A M, Bessant, D A, Bhattacharya, S S, Bird, A C
Published in Archives of ophthalmology (1960) (01.10.1999)
Published in Archives of ophthalmology (1960) (01.10.1999)
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Journal Article
Molecular genetics and prospects for therapy of the inherited retinal dystrophies
Bessant, David A.R, Ali, Robin R, Bhattacharya, Shomi S
Published in Current Opinion in Genetics & Development (01.06.2001)
Published in Current Opinion in Genetics & Development (01.06.2001)
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Book Review
Journal Article
A mutation in NRL is associated with autosomal dominant retinitis pigmentosa
Swaroop, Anand, Bhattacharya, Shomi S, Bessant, David A.R, Payne, Annette M, Mitton, Kenneth P, Wang, Qing-Liang, Swain, Prabodha K, Plant, Catherine, Bird, Alan C, Zack, Donald J
Published in Nature genetics (01.04.1999)
Published in Nature genetics (01.04.1999)
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Journal Article
Spectrum of Mutations in USH2A in British Patients with Usher Syndrome Type II
Leroy, Bart P, Aragon-Martin, José A, Weston, Michael D, Bessant, David A.R, Willis, Catherine, Webster, Andrew R, Bird, Alan C, Kimberling, William J, Payne, Annette M, Bhattacharya, Shomi S
Published in Experimental eye research (01.05.2001)
Published in Experimental eye research (01.05.2001)
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Journal Article
Founder Effect, Seen in the British Population, of the 172 Peripherin/RDS Mutation—and Further Refinement of Genetic Positioning of the Peripherin/RDS Gene
Payne, Annette M., Downes, Susan M., Bessant, David A.R., Bird, Alan C., Bhattacharya, Shomi S.
Published in American journal of human genetics (01.01.1998)
Published in American journal of human genetics (01.01.1998)
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Journal Article
Refinement of the Locus for Autosomal Recessive Retinitis Pigmentosa (RP25) Linked to Chromosome 6q in a Family of Pakistani Origin
Khaliq, Shagufta, Hameed, Abdul, Ismail, Muhammed, Mehdi, S. Qasim, Bessant, David A.R., Payne, Annette M., Bhattacharya, Shomi S.
Published in American journal of human genetics (01.08.1999)
Published in American journal of human genetics (01.08.1999)
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Journal Article