Payne AM - Search Results

1

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.

2

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

3

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.

4

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: payne am. Arch Ophthalmol. 1999 Oct;117(10):1373-83. doi: 10.1001/archopht.117.10.1373. Arch Ophthalmol. 1999. PMID: 10532447

5

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

6

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.

7

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

Bessant DA, Payne AM, Plant C, Bird AC, Bhattacharya SS. Bessant DA, et al. Among authors: payne am. J Med Genet. 1998 Sep;35(9):773-4. doi: 10.1136/jmg.35.9.773. J Med Genet. 1998. PMID: 9733039 Free PMC article.

8

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

Payne AM, Downes SM, Bessant DA, Plant C, Moore T, Bird AC, Bhattacharya SS. Payne AM, et al. J Med Genet. 1999 Sep;36(9):691-3. J Med Genet. 1999. PMID: 10507726 Free PMC article.

9

Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies.

Payne AM, Morris AG, Downes SM, Johnson S, Bird AC, Moore AT, Bhattacharya SS, Hunt DM. Payne AM, et al. J Med Genet. 2001 Sep;38(9):611-4. doi: 10.1136/jmg.38.9.611. J Med Genet. 2001. PMID: 11565546 Free PMC article. No abstract available.

10

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.

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