Analysis of predictors of success in the MRCP (UK) PACES examination in candidates attending a revision course

Por Bessant, R, Bessant, D, Chesser, A, Coakley, G
Publicado em 2006

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

Por Payne, A., Downes, S., Bessant, D., Plant, C., Moore, T., Bird, A., Bhattacharya, S.
Publicado em 1999

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

Por Bessant, D A, Payne, A M, Plant, C, Bird, A C, Bhattacharya, S S
Publicado em 1998

Founder effect, seen in the British population, of the 172 peripherin/RDS mutation-and further refinement of genetic positioning of the peripherin/RDS gene.

Por Payne, A M, Downes, S M, Bessant, D A, Bird, A C, Bhattacharya, S S
Publicado em 1998

Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32

Por Bessant, D., Anwar, K., Khaliq, S., Hameed, A., Ismail, M, Payne, A., Mehdi, S, Bhattacharya, S.
Publicado em 1999

A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32.

Por Bessant, D A, Khaliq, S, Hameed, A, Anwar, K, Mehdi, S Q, Payne, A M, Bhattacharya, S S
Publicado em 1998

Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin.

Por Khaliq, S, Hameed, A, Ismail, M, Mehdi, S Q, Bessant, D A, Payne, A M, Bhattacharya, S S
Publicado em 1999

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

Por BESSANT, D., PAYNE, A., SNOW, B., ANTINOLO, G., MEHDI, S, BIRD, A., SIDEROVSKI, D., BHATTACHARYA, S.
Publicado em 2000

A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q.

Por Papaioannou, M, Bessant, D, Payne, A, Bellingham, J, Rougas, C, Loutradis-Anagnostou, A, Gregory-Evans, C, Balassopoulou, A, Bhattacharya, S
Publicado em 1998