ORA - Oxford University Research Archive

1 - 10 of 10

1

Journal article

Ocular coloboma: a reassessment in the age of molecular neuroscience.

Gregory-Evans, CY, Williams, MJ, Halford, S, et al.
2004-12-05

2

Journal article

Imaging studies in congenital anophthalmia reveal preservation of brain architecture in 'visual' cortex.

Bridge, H, Cowey, A, Ragge, N, et al.
2009-12-05

3

Journal article

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen.

Bogani, D, Willoughby, C, Davies, J, et al.
2005-08-05

4

Journal article

Language networks in anophthalmia: maintained hierarchy of processing in 'visual' cortex.

Watkins, KE, Cowey, A, Alexander, I, et al.
2012-05-05

5

Journal article

Parent-of-origin effects in SOX2 anophthalmia syndrome.

Osborne, RJ, Kurinczuk, JJ, Ragge, NK
2011

6

Journal article

Visual callosal topography in the absence of retinal input.

Bock, AS, Saenz, M, Tungaraza, R, et al.
2013-11-05

7

Journal article

The fate of the oculomotor system in clinical bilateral anophthalmia.

Bridge, H, Ragge, N, Jenkinson, N, et al.
2012-05-05

8

Journal article

Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.

Rainger, J, Pehlivan, D, Johansson, S, et al.
2014-06-05

9

Journal article

Early auditory processing in area V5/MT+ of the congenitally blind brain.

Watkins, KE, Shakespeare, TJ, O'Donoghue, MC, et al.
2013-11-05

10

Journal article

Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes.

Engelen, E, Akinci, U, Bryne, JC, et al.
2011-06-05

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