Showing 1 - 3 results of 3 for search 'Inglehearn, C', query time: 0.02s
Refine Results
-
1
Amelogenesis Imperfecta; Genes, Proteins, and Pathways. by Smith, C, Poulter, J, Antanaviciute, A, Kirkham, J, Brookes, S, Inglehearn, C, Mighell, A
Published 2017Journal article -
2
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR). by Poulter, J, Davidson, A, Ali, M, Gilmour, D, Parry, D, Mintz-Hittner, H, Carr, I, Bottomley, H, Long, V, Downey, L, Sergouniotis, P, Wright, G, Maclaren, R, Moore, A, Webster, A, Inglehearn, C, Toomes, C
Published 2012Journal article -
3
Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data by Pontikos, N, Yu, J, Moghul, I, Withington, L, Blanco-Kelly, F, Vulliamy, T, Wong, T, Murphy, C, Cipriani, V, Fiorentino, A, Arno, G, Greene, D, Jacobsen, J, Clark, T, Gregory, D, Nemeth, A, Halford, S, Inglehearn, C, Downes, S, Black, G, Webster, A, Hardcastle, A, Plagnol, V
Published 2017Journal article