Showing 1 - 3 results of 3 for search 'van der Velde-Visser, S', query time: 0.02s
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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 1995Journal article -
2
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 2004Journal article -
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Impaired ABCA1/ABCG1-mediated lipid efflux in the mouse retinal pigment epithelium (RPE) leads to retinal degeneration by Federica Storti, Katrin Klee, Vyara Todorova, Regula Steiner, Alaa Othman, Saskia van der Velde-Visser, Marijana Samardzija, Isabelle Meneau, Maya Barben, Duygu Karademir, Valda Pauzuolyte, Sanford L Boye, Frank Blaser, Christoph Ullmer, Joshua L Dunaief, Thorsten Hornemann, Lucia Rohrer, Anneke den Hollander, Arnold von Eckardstein, Jürgen Fingerle, Cyrille Maugeais, Christian Grimm
Published 2019-03-01
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