Search Results - "Wiszniewski, Wojtek"

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  1. 1
    Refined Genetic and Physical Localization of the Wagner Disease (WGN1) Locus and the Genes CRTL1 and CSPG2 to a 2- to 2.5-cM Region of Chromosome 5q14.3

    Refined Genetic and Physical Localization of the Wagner Disease (WGN1) Locus and the Genes CRTL1 and CSPG2 to a 2- to 2.5-cM Region of Chromosome 5q14.3 by Perveen, Rahat, Hart-Holden, Niki, Dixon, Michael J., Wiszniewski, Wojtek, Fryer, Alan E., Brunner, Han G., Pinkners, Alfred J.L.H., van Beersum, Sylvie E.C., Black, Graeme C.M.

    Published in Genomics (San Diego, Calif.) (15-04-1999)
    “…Wagner syndrome (WGN1; MIM 143200), an autosomal dominant vitreoretinopathy characterized by chorioretinal atrophy, cataract, and retinal detachment, is linked…”
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  2. 2
    A novel hereditary developmental vitreoretinopathy with multiple ocular abnormalities localizing to a 5-cM region of chromosome 5q13-q14

    A novel hereditary developmental vitreoretinopathy with multiple ocular abnormalities localizing to a 5-cM region of chromosome 5q13-q14 by Black, G C, Perveen, R, Wiszniewski, W, Dodd, C L, Donnai, D, McLeod, D

    Published in Ophthalmology (Rochester, Minn.) (01-11-1999)
    “…To undertake a clinical and molecular analysis of a previously unpublished kindred with a phenotypically distinct vitreoretinopathy characterized by associated…”
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