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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 AM, Downes SM, Bessant DA, Bird AC, Bhattacharya SS. Payne AM, et al. Among authors: bessant da. Am J Hum Genet. 1998 Jan;62(1):192-5. doi: 10.1086/301679. Am J Hum Genet. 1998. PMID: 9443872 Free PMC article. No abstract available.
Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin.
Khaliq S, Hameed A, Ismail M, Mehdi SQ, Bessant DA, Payne AM, Bhattacharya SS. Khaliq S, et al. Among authors: bessant da. Am J Hum Genet. 1999 Aug;65(2):571-4. doi: 10.1086/302493. Am J Hum Genet. 1999. PMID: 10417302 Free PMC article. No abstract available.
NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies.
Bessant DA, Payne AM, Plant C, Bird AC, Swaroop A, Bhattacharya SS. Bessant DA, et al. Eur J Hum Genet. 2000 Oct;8(10):783-7. doi: 10.1038/sj.ejhg.5200538. Eur J Hum Genet. 2000. PMID: 11039579
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 AM, Downes SM, Bessant DA, Taylor R, Holder GE, Warren MJ, Bird AC, Bhattacharya SS. Payne AM, et al. Among authors: bessant da. Hum Mol Genet. 1998 Feb;7(2):273-7. doi: 10.1093/hmg/7.2.273. Hum Mol Genet. 1998. PMID: 9425234
A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32.
Bessant DA, Khaliq S, Hameed A, Anwar K, Mehdi SQ, Payne AM, Bhattacharya SS. Bessant DA, et al. Am J Hum Genet. 1998 May;62(5):1113-6. doi: 10.1086/301843. Am J Hum Genet. 1998. PMID: 9545413 Free PMC article.
A mutation in NRL is associated with autosomal dominant retinitis pigmentosa.
Bessant DA, Payne AM, Mitton KP, Wang QL, Swain PK, Plant C, Bird AC, Zack DJ, Swaroop A, Bhattacharya SS. Bessant DA, et al. Nat Genet. 1999 Apr;21(4):355-6. doi: 10.1038/7678. Nat Genet. 1999. PMID: 10192380 No abstract available.
Spectrum of mutations in USH2A in British patients with Usher syndrome type II.
Leroy BP, Aragon-Martin JA, Weston MD, Bessant DA, Willis C, Webster AR, Bird AC, Kimberling WJ, Payne AM, Bhattacharya SS. Leroy BP, et al. Among authors: bessant da. Exp Eye Res. 2001 May;72(5):503-9. doi: 10.1006/exer.2000.0978. Exp Eye Res. 2001. PMID: 11311042
Molecular genetics and prospects for therapy of the inherited retinal dystrophies.
Bessant DA, Ali RR, Bhattacharya SS. Bessant DA, et al. Curr Opin Genet Dev. 2001 Jun;11(3):307-16. doi: 10.1016/s0959-437x(00)00195-7. Curr Opin Genet Dev. 2001. PMID: 11377968 Review.
Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 families.
Downes SM, Fitzke FW, Holder GE, Payne AM, Bessant DA, Bhattacharya SS, Bird AC. Downes SM, et al. Among authors: bessant da. Arch Ophthalmol. 1999 Oct;117(10):1373-83. doi: 10.1001/archopht.117.10.1373. Arch Ophthalmol. 1999. PMID: 10532447
Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r).
Bessant DA, Payne AM, Snow BE, AntiƱo G, Mehdi SQ, Bird AC, Siderovski DP, Bhattacharya SS. Bessant DA, et al. J Med Genet. 2000 May;37(5):384-7. doi: 10.1136/jmg.37.5.384. J Med Genet. 2000. PMID: 10905894 Free PMC article. No abstract available.
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