Gene Conversion between Red and Defective Green Opsin Gene in Blue Cone Monochromacy von REYNIERS, EDWIN, VANTHIENEN, MARIE-NOËLLE, MEIRE, FRANÇOISE, DEBOULLE, KRISTEL, DEVRIES, KRISTINE, KESTELIJN, PHILIP, WILLEMS, PATRICK J.

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Fmr1 knockout mice: A model to study fragile X mental retardation von The Dutch-Belgian Fragile X Consorthium, Bakker, Cathy E., Verheij, Coleta, Willemsen, Rob, van der Helm, Robert, Oerlemans, Frank, Vermey, Marcel, Bygrave, Anne, Hoogeveen, AndréT., Oostra, Ben A., Reyniers, Edwin, De Boule, Kristel, D'Hooge, Rudi, Cras, Patrick, van Velzen, Désiré, Nagels, Guy, Martin, Jean-Jacques, De Deyn, Peter P., Darby, John K., Willems, Patrick J.

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

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

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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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Alternative splicing in the fragile X gene FMR1 von Verkerk, Annemieke J.M.H., de Graaff, Esther, De Boulle, Kristel, Eichler, Evan E., Konecki, David S., Reyniers, Edwin, Manca, Antonella, Poustka, Annemarie, Willems, Patrick J., Nelson, David L., Oostra, Ben A.

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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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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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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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Mean corpuscular hemoglobin is not increased in Fmr1 knockout mice von REYNIERS, E, VAN BOCKSTAELE, D. R, DE BOULLE, K, KOOY, R. F, BAKKER, C. E, OOSTRA, B. A, WILLEMS, P. J

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Long-term potentiation in the hippocampus of fragile X knockout mice von Godfraind, Jean-Marie, Reyniers, Edwin, De Boulle, Kristel, D'Hooge, Rudi, De Deyn, Peter P., Bakker, Cathy E., Oostra, Ben A., Kooy, R. Frank, Willems, Patrick J.

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Transgenic mouse model for the fragile X syndrome von Kooy, R. Frank, D'Hooge, Rudi, Reyniers, Edwin, Bakker, Cathy E., Nagels, Guy, De Boulle, Kristel, Storm, Katrien, Clincke, Gilbert, De Deyn, Peter P., Oostra, Ben A., Willems, Patrick J.

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Severe mental retardation and macroorchidism without mutation in the FMR1 gene von Reyniers, Edwin, Wolff, Gerhard, Tariverdian, Gholamali, De Boulle, Kristel, Storm, Katrien, Kooy, R. Frank, Willems, Patrick J.

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