Webster AR - Search Results

1

Variability of retinopathy consequent upon novel mutations in LAMA1.

Schiff ER, Aychoua N, Nutan S, Davagnanam I, Moore AT, Robson AG, Patel CK, Webster AR, Arno G. Schiff ER, et al. Among authors: webster ar. Ophthalmic Genet. 2022 Oct;43(5):671-678. doi: 10.1080/13816810.2022.2076283. Epub 2022 May 26. Ophthalmic Genet. 2022. PMID: 35616092

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

Risk of multisystem disease in isolated ocular angioma (haemangioblastoma).

Webster AR, Maher ER, Bird AC, Moore AT. Webster AR, et al. J Med Genet. 2000 Jan;37(1):62-3. doi: 10.1136/jmg.37.1.62. J Med Genet. 2000. PMID: 10691410 Free PMC article. No abstract available.

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

365 results

Search Page