Works matching AU Harrison, Wilbur


Results: 14
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    Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis.

    Published in:
    Nature Genetics, 2000, v. 24, n. 1, p. 79, doi. 10.1038/71732
    By:
    • Sohocki, Melanie M.;
    • Bowne, Sara J.;
    • Sullivan, Lori S.;
    • Blackshaw, Seth;
    • Cepko, Constance L.;
    • Payne, Annette M.;
    • Bhattacharya, Shomi S.;
    • Khaliq, Shagufta;
    • Qasim Mehdi, S.;
    • Birch, David G.;
    • Harrison, Wilbur R.;
    • Elder, Frederick F.B.;
    • Heckenlively, John R.;
    • Daiger, Stephen P.
    Publication type:
    Article
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    A transgenic insertion causing cryptorchidism in mice.

    Published in:
    Genesis: The Journal of Genetics & Development, 2001, v. 30, n. 1, p. 26, doi. 10.1002/gene.1029
    By:
    • Overbeek, Paul A.;
    • Gorlov, Ivan P.;
    • Sutherland, Richard W.;
    • Houston, John B.;
    • Harrison, Wilbur R.;
    • Boettger-Tong, Holly L.;
    • Bishop, Colin E.;
    • Agoulnik, Alexander I.
    Publication type:
    Article
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