X-linked Retinitis Pigmentosa: RPGR Mutations in Most Families with Definite X Linkage and Clustering of Mutations in a Short Sequence Stretch of Exon ORF15 von Bader, Ingrid, Brandau, Oliver, Achatz, Helene, Apfelstedt-Sylla, Eckart, Hergersberg, Martin, Lorenz, Birgit, Wissinger, Bernd, Wittwer, Barbel, Rudolph, Gunther, Meindl, Alfons, Meitinger, Thomas

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Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain von Gaudenz, Karin, Roessler, Erich, Quaderi, Nandita, Franco, Brunella, Feldman, George, Gasser, David L., Wittwer, Bärbel, Montini, Eugenio, Opitz, John M., Ballabio, Andrea, Muenke, Maximilian

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A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa von Meindl, Alfons, Carvalho, Maria Raquel S., Herrmann, Klaus, Lorenz, Bettina, Achatz, Helene, Lorenz, Birgit, Apfelstedt-Sylla, Eckart, Wittwer, Bärbel, Ross, Mark, Meitinger, Thomas

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FURTHER LOCALIZATION OF X-LINKED HYDROCEPHALUS IN THE CHROMOSOMAL REGION-XQ28 von WILLEMS, PJ, VITS, L, RAEYMAEKERS, P, BEUTEN, J, COUCKE, P, HOLDEN, JJA, VAN BROECKHOVEN, C, WARREN, ST, SAGI, M, ROBINSON, D, DENNIS, N, FRIEDMAN, KJ, MAGNAY, D, LYONNET, S, WHITE, BN, WITTWER, BH, AYLSWORTH, AS, REICKE, S

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Submicroscopic deletion in 14q32.3 through a de novo tandem translocation between 14q and 21p von Meschede, Dieter, Exeler, Rita, Wittwer, Bärbel, Horst, Jürgen

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New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3 von Wittwer, Bärbel, Kircheisen, Renate, Leutelt, Jutta, Orth, Ulrike, Gal, Andreas

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