Showing 1 - 3 results of 3 for search 'van der Velde-Visser, S', query time: 0.03s Refine Results
  1. 1
    Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290

    Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290 by Rob WJ Collin, Anneke I den Hollander, Saskia D van der Velde-Visser, Jeannette Bennicelli, Jean Bennett, Frans PM Cremers

    Published 2012-01-01
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    Article
  2. 2
    A high-resolution interval map of the q21 region of the human X chromosome.

    A high-resolution interval map of the q21 region of the human X chromosome. by Philippe, C, Arnould, C, Sloan, F, van Bokhoven, H, van der Velde-Visser, S, Chery, M, Ropers, H, Gilgenkrantz, S, Monaco, A, Cremers, F

    Published 1995
    Journal article
  3. 3
    CRB1 mutation spectrum in inherited retinal dystrophies.

    CRB1 mutation spectrum in inherited retinal dystrophies. by den Hollander, A, Davis, J, van der Velde-Visser, S, Zonneveld, M, Pierrottet, C, Koenekoop, R, Kellner, U, van den Born, L, Heckenlively, JR, Hoyng, C, Handford, P, Roepman, R, Cremers, F

    Published 2004
    Journal article

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