Search results - ORA - Oxford University Research Archive

1 - 8 of 8

1

Conference item

The protect (prostate testing for cancer and treatment) study: Advanced cases found through a UK screening study

Neal, D, Moore, A, Hamdy, F, et al.
2006-04-01

2

Journal article

Macular function assessed by microperimetry in patients with enhanced S-cone syndrome.

Sohn, E, Chen, F, Rubin, G, et al.
2010-06-01

3

Journal article

Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy.

Tan, M, Mackay, D, Cowing, J, et al.
2012-01-01

4

Journal article

Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR).

Poulter, J, Davidson, A, Ali, M, et al.
2012-05-01

5

Journal article

X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene.

McClements, M, Davies, W, Michaelides, M, et al.
2013-03-01

6

Journal article

Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.

McClements, M, Davies, W, Michaelides, M, et al.
2013-02-15

7

Journal article

Population-based prostate-specific antigen testing in the UK leads to a stage migration of prostate cancer.

Moore, A, Dimitropoulou, P, Lane, A, et al.
2009-12-01

8

Journal article

ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicing.

Burgess, R, Maclaren, R, Davidson, A, et al.
2009-09-01

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