Showing 1 - 3 results of 3 for search 'Inglehearn, C' Skip to content
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  • Inglehearn, C
Showing 1 - 3 results of 3 for search 'Inglehearn, C', query time: 0.02s Refine Results
  1. 1
    Amelogenesis Imperfecta; Genes, Proteins, and Pathways.

    Amelogenesis Imperfecta; Genes, Proteins, and Pathways. by Smith, C, Poulter, J, Antanaviciute, A, Kirkham, J, Brookes, S, Inglehearn, C, Mighell, A

    Published 2017
    Journal article
  2. 2
    Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR).

    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 2012
    Journal article
  3. 3
    Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data

    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 2017
    Journal article

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