Items where authors include "Maconachie, G.D.E."

Article

Kuht, H.J., Maconachie, G.D.E. orcid.org/0000-0001-9131-3480, Han, J. et al. (36 more authors) (2022) Genotypic and phenotypic spectrum of foveal hypoplasia : a multicenter study. Ophthalmology, 129 (6). pp. 708-718. ISSN 0161-6420

Thomas, M.G., Maconachie, G.D.E. orcid.org/0000-0001-9131-3480, Kuht, H.J. et al. (10 more authors) (2021) Optic nerve head and retinal abnormalities associated with congenital fibrosis of the extraocular muscles. International Journal of Molecular Sciences, 22 (5). 2575.

Kuht, H.J., Han, J., Maconachie, G.D.E. orcid.org/0000-0001-9131-3480 et al. (12 more authors) (2020) SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization. Human Molecular Genetics, 29 (18). pp. 2989-3002. ISSN 0964-6906

Maconachie, G.D.E. and Gottlob, I. (2015) The challenges of amblyopia treatment. Biomedical Journal, 38 (6). pp. 510-516. ISSN 2319-4170