Search Results - Bessant, David A.R

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  1. 1
    Molecular genetics and prospects for therapy of the inherited retinal dystrophies

    Molecular genetics and prospects for therapy of the inherited retinal dystrophies by Bessant, David A.R, Ali, Robin R, Bhattacharya, Shomi S

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  2. 2
    Spectrum of Mutations in USH2A in British Patients with Usher Syndrome Type II

    Spectrum of Mutations in USH2A in British Patients with Usher Syndrome Type II by 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

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  3. 3
    Founder Effect, Seen in the British Population, of the 172 Peripherin/RDS Mutation—and Further Refinement of Genetic Positioning of the Peripherin/RDS Gene

    Founder Effect, Seen in the British Population, of the 172 Peripherin/RDS Mutation—and Further Refinement of Genetic Positioning of the Peripherin/RDS Gene by Payne, Annette M., Downes, Susan M., Bessant, David A.R., Bird, Alan C., Bhattacharya, Shomi S.

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  4. 4
    A Locus for Autosomal Recessive Congenital Microphthalmia Maps to Chromosome 14q32

    A Locus for Autosomal Recessive Congenital Microphthalmia Maps to Chromosome 14q32 by Bessant, David A.R., Khaliq, Shagufta, Hameed, Abdul, Anwar, Khalid, Mehdi, S. Qasim, Payne, Annette M., Bhattacharya, Shomi S.

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  5. 5
    Refinement of the Locus for Autosomal Recessive Retinitis Pigmentosa (RP25) Linked to Chromosome 6q in a Family of Pakistani Origin

    Refinement of the Locus for Autosomal Recessive Retinitis Pigmentosa (RP25) Linked to Chromosome 6q in a Family of Pakistani Origin by Khaliq, Shagufta, Hameed, Abdul, Ismail, Muhammed, Mehdi, S. Qasim, Bessant, David A.R., Payne, Annette M., Bhattacharya, Shomi S.

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  6. 6
    A Mutation in Guanylate Cyclase Activator 1A (GUCA1A) in an Autosomal Dominant Cone Dystrophy Pedigree Mapping to a New Locus on Chromosome 6p21.1

    A Mutation in Guanylate Cyclase Activator 1A (GUCA1A) in an Autosomal Dominant Cone Dystrophy Pedigree Mapping to a New Locus on Chromosome 6p21.1 by Payne, Annette M., Downes, Susan M., Bessant, David A.R., Taylor, Rachel, Holder, Graham E., Warren, Martin J., Bird, Alan C., Bhattacharya, Shomi S.

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  7. 7
    Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu)

    Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu) by Bessant, David A.R., Khaliq, Shagufta, Hameed, Abdul, Anwar, Khalid, Payne, Annette M., Mehdi, S. Qasim, Bhattacharya, Shomi S.

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  8. 8
    Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies

    Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies by Payne, Annette M, Downes, Susan M, Bessant, David A R, Plant, Catherine, Moore, Tony, Bird, Alan C, Bhattacharya, Shomi S

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  9. 9
    Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32

    Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32 by Bessant, David A R, Anwar, Khalid, Khaliq, Shagufta, Hameed, Abdul, Ismail, M, Payne, Annette M, Mehdi, S Qasim, Bhattacharya, Shomi S

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  10. 10
    Further refinement of the Usher 2A locus at 1q41

    Further refinement of the Usher 2A locus at 1q41 by Bessant, D A, Payne, A M, Plant, C, Bird, A C, Bhattacharya, S S

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  11. 11
    Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r)

    Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r) by BESSANT, DAVID A R, PAYNE, ANNETTE M, SNOW, BRYAN E, ANTIÑOLO, GUILLERMO, MEHDI, S QASIM, BIRD, ALAN C, SIDEROVSKI, DAVID P, BHATTACHARYA, SHOMI S

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