Webster AR - Search Results

1

The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56.

Almoallem B, Arno G, De Zaeytijd J, Verdin H, Balikova I, Casteels I, de Ravel T, Hull S, Suzani M, Destrée A, Peng M, Williams D, Ainsworth JR, Webster AR, Leroy BP, Moore AT, De Baere E. Almoallem B, et al. Among authors: webster ar. Sci Rep. 2020 Jan 28;10(1):1289. doi: 10.1038/s41598-019-57338-2. Sci Rep. 2020. PMID: 31992737 Free PMC article.

2

Ischaemic retinopathy occurring in patients receiving bone marrow allografts and campath-1G: a clinicopathological study.

Webster AR, Anderson JR, Richards EM, Moore AT. Webster AR, et al. Br J Ophthalmol. 1995 Jul;79(7):687-91. doi: 10.1136/bjo.79.7.687. Br J Ophthalmol. 1995. PMID: 7662637 Free PMC article.

3

Ocular malformations and the fruits of developmental genetics.

Webster AR, Moore AT. Webster AR, et al. Eye (Lond). 1994;8 ( Pt 5):v. doi: 10.1038/eye.1994.123. Eye (Lond). 1994. PMID: 7835439 No abstract available.

4

Clinical features and molecular genetics of Von Hippel-Lindau disease.

Maher ER, Webster AR, Moore AT. Maher ER, et al. Among authors: webster ar. Ophthalmic Genet. 1995 Sep;16(3):79-84. doi: 10.3109/13816819509059966. Ophthalmic Genet. 1995. PMID: 8556282 Review.

5

Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.

Maher ER, Webster AR, Richards FM, Green JS, Crossey PA, Payne SJ, Moore AT. Maher ER, et al. Among authors: webster ar. J Med Genet. 1996 Apr;33(4):328-32. doi: 10.1136/jmg.33.4.328. J Med Genet. 1996. PMID: 8730290 Free PMC article.

6

An analysis of phenotypic variation in the familial cancer syndrome von Hippel-Lindau disease: evidence for modifier effects.

Webster AR, Richards FM, MacRonald FE, Moore AT, Maher ER. Webster AR, et al. Am J Hum Genet. 1998 Oct;63(4):1025-35. doi: 10.1086/302037. Am J Hum Genet. 1998. PMID: 9758595 Free PMC article.

7

A clinical and molecular genetic analysis of solitary ocular angioma.

Webster AR, Maher ER, Bird AC, Gregor ZJ, Moore AT. Webster AR, et al. Ophthalmology. 1999 Mar;106(3):623-9. doi: 10.1016/S0161-6420(99)90127-6. Ophthalmology. 1999. PMID: 10080225

8

Clinical characteristics of ocular angiomatosis in von Hippel-Lindau disease and correlation with germline mutation.

Webster AR, Maher ER, Moore AT. Webster AR, et al. Arch Ophthalmol. 1999 Mar;117(3):371-8. doi: 10.1001/archopht.117.3.371. Arch Ophthalmol. 1999. PMID: 10088816

9

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: webster ar. Exp Eye Res. 2001 May;72(5):503-9. doi: 10.1006/exer.2000.0978. Exp Eye Res. 2001. PMID: 11311042

10

Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa.

Chakarova CF, Hims MM, Bolz H, Abu-Safieh L, Patel RJ, Papaioannou MG, Inglehearn CF, Keen TJ, Willis C, Moore AT, Rosenberg T, Webster AR, Bird AC, Gal A, Hunt D, Vithana EN, Bhattacharya SS. Chakarova CF, et al. Among authors: webster ar. Hum Mol Genet. 2002 Jan 1;11(1):87-92. doi: 10.1093/hmg/11.1.87. Hum Mol Genet. 2002. PMID: 11773002

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