Originalkatalog | Verfügbarkeit prüfen

Novel missense mutation in the caveolin-3 gene in a Belgian family with rippling muscle disease.

Van den Bergh, Peter, Gerard, Jean-Marc, Elosegi, J A, Manto, M U, Kubisch, C., Schoser, B G H
2004

Originalkatalog | Verfügbarkeit prüfen

The prevalence of nine genetic disorders in a dog population from Belgium, the Netherlands and Germany

Broeckx, Bart, Coopman, Frank, Verhoeven, Geert, Van Haeringen, Wim, van de Goor, Leanne, Bosmans, Tim, Gielen, Ingrid, Saunders, Jimmy, Soetaert, Sandra, van Bree, Henri, Van Neste, Christophe, Van Nieuwerburgh, Filip, Van Ryssen, Bernadette, Verelst, Elien, Van Steendam, Katleen, Deforce, Dieter
2013

Originalkatalog | Verfügbarkeit prüfen

Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

van Leeuwen, Elisabeth M, Karssen, Lennart C, Deelen, Joris, Isaacs, Aaron, Medina-Gomez, Carolina, Mbarek, Hamdi, Kanterakis, Alexandros, Trompet, Stella, Postmus, Iris, Verweij, Niek, van Enckevort, David J, Huffman, Jennifer E, White, Charles C, Feitosa, Mary F, Bartz, Traci M, Manichaikul, Ani, Joshi, Peter K, Peloso, Gina M, Deelen, Patrick, van Dijk, Freerk, Willemsen, Gonneke, de Geus, Eco J, Milaneschi, Yuri, Penninx, Brenda WJH, Francioli, Laurent C, Menelaou, Androniki, Pulit, Sara L, Rivadeneira, Fernando, Hofman, Albert, Oostra, Ben A, Franco, Oscar H, Leach, Irene Mateo, Beekman, Marian, de Craen, Anton JM, Uh, Hae-Won, Trochet, Holly, Hocking, Lynne J, Porteous, David J, Sattar, Naveed, Packard, Chris J, Buckley, Brendan M, Brody, Jennifer A, Bis, Joshua C, Rotter, Jerome I, Mychaleckyj, Josyf C, Campbell, Harry, Duan, Qing, Lange, Leslie A, Wilson, James F, Hayward, Caroline, Polasek, Ozren, Vitart, Veronique, Rudan, Igor, Wright, Alan F, Rich, Stephen S, Psaty, Bruce M, Borecki, Ingrid B, Kearney, Patricia M, Stott, David J, Adrienne Cupples, L, Jukema, J Wouter, van der Harst, Pim, Sijbrands, Eric J, Hottenga, Jouke-Jan, Uitterlinden, Andre G, Swertz, Morris A, van Ommen, Gert-Jan B, de Bakker, Paul IW, Eline Slagboom, P, Boomsma, Dorret I, Wijmenga, Cisca, van Duijn, Cornelia M
Veröffentlicht in: Nature Communications, vol 6, iss 1;
2015

Originalkatalog | Verfügbarkeit prüfen

Mutations in splicing factor genes are a major cause of autosomal dominant retinitis pigmentosa in Belgian families

Van Cauwenbergh, Caroline, Coppieters, Frauke, Roels, Dimitri, De Jaegere, Sarah, Flipts, Helena, De Zaeytijd, Julie, WALRAEDT, SOPHIE, Claes, Charlotte, Fransen, Erik, Van Camp, Guy, Depasse, Fanny, Casteels, Ingele, de Ravel, Thomy, Leroy, Bart, De Baere, Elfride
2017