Search Results - Forman, O.P

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  1. 1
    Canine RPGRIP1 mutation establishes cone–rod dystrophy in miniature longhaired dachshunds as a homologue of human Leber congenital amaurosis

    Canine RPGRIP1 mutation establishes cone–rod dystrophy in miniature longhaired dachshunds as a homologue of human Leber congenital amaurosis by Mellersh, C.S., Boursnell, M.E.G., Pettitt, L., Ryder, E.J., Holmes, N.G., Grafham, D., Forman, O.P., Sampson, J., Barnett, K.C., Blanton, S., Binns, M.M., Vaudin, M.

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  2. 2
    Simultaneous identification of every gene in Streptococcus equi subspecies equi by TraDIS

    Simultaneous identification of every gene in Streptococcus equi subspecies equi by TraDIS by Charbonneau, A.R.L., Waller, A.S., Forman, O.P., Robinson, C., Steward, K.F.

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  3. 3
    Optimisation of a live attenuated vaccine against strangles

    Optimisation of a live attenuated vaccine against strangles by Robinson, C., Charbonneau, A.R.L., Forman, O.P., Steward, K.F., Cain, A.K., Waller, A.S.

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  4. 4
    Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriers

    Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriers by Forman, O.P, Boursnell, M.E.G, Dunmore, B.J, Stendall, N, Sluis, B. van de, Fretwell, N, Jones, C, Wijmenga, C, Rothuizen, J, Oost, B.A. van

    Published in Animal genetics
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