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The British Journal of Ophthalmology|January 25, 2005
A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1M Michaelides, G E Holder, D M Hunt, et al.The British Journal of Ophthalmology|May 12, 2011
High-resolution optical coherence tomography imaging in KCNV2 retinopathyPanagiotis I Sergouniotis, Graham E Holder, Anthony G Robson, et al.Clinical Nuclear Medicine|May 1, 1997
Scrotal pathology as the cause for hip pain. Diagnostic findings on bone scintigraphyD H Sheafor, L E Holder, D Thompson, et al.Journal of Molecular and Cellular Cardiology|April 4, 1998
A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathyR D Bies, M Maeda, S L Roberds, et al.Eye (London, England)|May 23, 2015
Congenital high myopia and central macular atrophy: a report of 3 familiesS Hull, A Kalhoro, J Marr, et al.Documenta Ophthalmologica. Advances in Ophthalmology|June 24, 2018
ISCEV extended protocol for the photopic On-Off ERGMaja Sustar, Graham E Holder, Jan Kremers, et al.Ophthalmic Genetics|April 16, 2026
A novel CEP78 variant and rod-cone dystrophy in non-consanguineous siblingsDominic S Ting, Graham E Holder, Melissa C Tien, et al.Neurogenetics|July 8, 2009
Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorderMartin Poot, Vera Beyer, Ira Schwaab, et al.Investigative Ophthalmology & Visual Science|January 31, 2003
Electrophysiological and psychophysical differences between early- and late-onset strabismic amblyopiaAlison R Davis, John J Sloper, Majella M Neveu, et al.AIDS Care|December 16, 2015
Genitourinary Medicine staff knowledge about the risks of specific sexual behaviours in the transmission of HIVJ E Holder, D Shah, L Brewester, et al.Pageof 36