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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. 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.
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. Among authors: payne am. Eur J Hum Genet. 2000 Oct;8(10):783-7. doi: 10.1038/sj.ejhg.5200538. Eur J Hum Genet. 2000. PMID: 11039579
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: payne am. 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.
Molecular genetic study of autosomal dominant retinitis pigmentosa in Lithuanian patients.
Kucinskas V, Payne AM, Ambrasiene D, Jurgelevicius V, Steponaviciūte D, Arciuliene JV, Daktaraviciene E, Bhattacharya S. Kucinskas V, et al. Among authors: payne am. Hum Hered. 1999 Mar;49(2):71-4. doi: 10.1159/000022847. Hum Hered. 1999. PMID: 10077725
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. 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. Among authors: payne am. 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 new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q.
Papaioannou M, Bessant D, Payne A, Bellingham J, Rougas C, Loutradis-Anagnostou A, Gregory-Evans C, Balassopoulou A, Bhattacharya S. Papaioannou M, et al. J Med Genet. 1998 May;35(5):429-31. doi: 10.1136/jmg.35.5.429. J Med Genet. 1998. PMID: 9610810 Free PMC article.
Dominant optic atrophy: exclusion and fine genetic mapping of the candidate gene, HRY.
Votruba M, Payne A, Moore AT, Bhattacharya SS. Votruba M, et al. Mamm Genome. 1998 Oct;9(10):784-7. doi: 10.1007/s003359900867. Mamm Genome. 1998. PMID: 9745030
RP1 protein truncating mutations predominate at the RP1 adRP locus.
Payne A, Vithana E, Khaliq S, Hameed A, Deller J, Abu-Safieh L, Kermani S, Leroy BP, Mehdi SQ, Moore AT, Bird AC, Bhattacharya SS. Payne A, et al. Invest Ophthalmol Vis Sci. 2000 Dec;41(13):4069-73. Invest Ophthalmol Vis Sci. 2000. PMID: 11095597
An analysis of ABCR mutations in British patients with recessive retinal dystrophies.
Papaioannou M, Ocaka L, Bessant D, Lois N, Bird A, Payne A, Bhattacharya S. Papaioannou M, et al. Invest Ophthalmol Vis Sci. 2000 Jan;41(1):16-9. Invest Ophthalmol Vis Sci. 2000. PMID: 10634594
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