Two brothers with mental retardation discordant for the Fragile-X syndrome von van Roy, Bernadette C., Willems, Patrick J., Vits, Lieve J., Ceulemans, Berten P., Coucke, Paul J., van der Auwera, Bart J., Lormans, Jacques A. G., Dumon, Jan E.

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THU-249 The role of the ferroptosis brake glutathione peroxidase 4 in a preclinical model of metabolic dysfunction-associated steatohepatitis von Peleman, Cédric, Veeckmans, Geraldine, Hassannia, Behrouz, Vits, Lieve, Van San, Emily, De Man, Joris, Van Eyck, Annelies, Kwanten, Wilhelmus J., Vonghia, Luisa, Driessen, Ann, De Winter, Benedicte, Van Steenkiste, Christophe, Francque, Sven, Vanden Berghe, Tom

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CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1 von Fransen, E, Lemmon, V, Van Camp, G, Vits, L, Coucke, P, Willems, P J

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L1-Associated Diseases: Clinical Geneticists Divide, Molecular Geneticists Unite von Fransen, Erik, Van Camp, Guy, Vits, Lieve, Willems, Patrick J.

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A point mutation in the FMR-1 gene associated with fragile X mental retardation von Van Roy, Bernadette, Willems, Patrick J, De Boulle, Kristel, Reyniers, Edwin, Hendrickx, Jan, Van Den Bos, Feikje, Verkerk, Annemieke J.M.H, Oostra, Ben A, Vits, Lieve, de Graaff, Esther

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Positional Cloning of a Gene Involved in Hereditary Multiple Exostoses von Wuyts, Wim, Van Hul, Wim, Wauters, Jan, Nemtsova, Marina, Reyniers, Edwin, Van Hul, Els, De Boulle, Kristel, de Vries, Bert B. A., Hendrickx, Jan, Herrygers, Ilde, Bossuyt, Paul, Balemans, Wendy, Fransen, Erik, Vits, Lieve, Coucke, Paul, Nowak, Norma J., Shows, Thomas B., Mallet, Laurence, van den Ouweland, Ans M. W., McGaughran, Julie, Halley, Dicky J. J., Willems, Patrick J.

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Genotype-phenotype correlation in L1 associated diseases von Fransen, E, Van Camp, G, D'Hooge, R, Vits, L, Willems, P J

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The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm von Willems, Patrick J, Reyniers, Edwin, De Boulle, Kristel, Oostra, Ben, Verkerk, Annemieke J.M.H, Velzen, Desirée Van, Jorens, Hugo Z.J, Darby, John K, Vits, Lieve, Roy, Bernadette Van, de Graaff, Esther

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MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM von Vits, Lieve, Van Camp, Guy, Coucke, Paul, Fransen, Erik, De Boulle, Kristel, Reyniers, Edwin, Korn, Bernhard, Poustka, Annemarie, Wilson, Golder, Schrander-Stumpel, Connie, Winter, Robin M, Schwartz, Charles, Willems, Patrick J

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A locus-specific mutation database for the neural cell adhesion molecule L1CAM (Xq28) von Van Camp, Guy, Fransen, Erik, Vits, Lieve, Raes, Geert, Willems, Patrick J.

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Evidence for somatic and germline mosaicism in CRASH syndrome von Vits, Lieve, Chitayat, David, van Camp, Guy, Holden, Jeanette J.A., Fransen, Erik, Willems, Patrick J.

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Segregation of the fragile X mutation from an affected male to his normal daughter von Willems, Patrick J., Roy, Bernadette Van, De Boulle, Kristel, Vits, Lieve, Reyniers, Edwin, Beck, Olivia, Dumon, Jan E., Verkerk, Annemieke, Oostra, Ben

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A duplication in the L1CAM gene associated with X-linked hydrocephalus von Darby, John, Holden, Jeanette, Willems, Patrick J, Munnich, Arnold, Camp, Guy Van, Lyonnet, Stanislas, Vits, Lieve, Coucke, Paul, Schrander-Stumpel, Connie

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X-linked hydrocephalus and MASA syndrome present in one family are due to a single missense mutation in exon 28 of the L1CAM gene von Fransen, Erik, Schrander-Stumpel, Connle, Vits, Lieve, Coucke, Paul, Van Camp, Guy, Willems, Patrick J.

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Further localization of X-linked hydrocephalus in the chromosomal region Xq28 von Willems, P J, Vits, L, Raeymaekers, P, Beuten, J, Coucke, P, Holden, J J, Van Broeckhoven, C, Warren, S T, Sagi, M, Robinson, D

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Founder effect in a Belgian-Dutch fragile X population von BUYLE, S, REYNIERS, E, VITS, L, DE BOULLE, K, HANDIG, I, WUYTS, F. L. E, DEELEN, W, HALLEY, D. J. J, OOSTRA, B. A, WILLEMS, P. J

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Apparent regression of the CGG repeat in FMR1 to an allele of normal size von Vits, L, De Boulle, K, Reyniers, E, Handig, I, Darby, J K, Oostra, B, Willems, P J

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Assignment of X-linked hydrocephalus to Xq28 by linkage analysis von Willems, Patrick J., Dijkstra, Irene, Van der Auwera, Bart J., Vits, Lieve, Coucke, Paul, Raeymaekers, Peter, Van Broeckhoven, Christine, Consalez, Giacomo G., Freeman, Sallie B., Warren, Stephen T., Brouwer, Oebele F., Brunner, Han G., Renier, Willy O., Van Elsen, August F., Dumon, Jan E.

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DXS89 (pTAK10) detects a homologous sequence on the Y chromosome von Hendrickx, Jan, Vits, Lieve, Willems, Patrick J.

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Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22 von Willems, Patrick J., Hendrickx, Jan, Van der Auwera, Bart J., Vits, Lieve, Raeymaekers, Peter, Coucke, Paul J., Van den Bergh, Inge, Berger, Ruud, Smit, G.Peter A., Van Broeckhoven, Christine, Kilimann, Manfred W., Van Elsen, August F., Fernandes, John F.

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