-
1
-
2by BLITTERSWIJK, Marka Van, ES, Michael A. Van, DE BAKKER, Paul I. W, VELDINK, Jan H, DEN BERG, Leonard H. Van, HENNEKAM, Eric A. M, DOOIJES, Dennis, RHEENEN, Wouter Van, MEDIC, Jelena, BOURQUE, Pierre R, SCHELHAAS, Helenius J, DER KOOI, Anneke J. Van, DE VISSER, MarianneGet full text
Published in Human molecular genetics
Article -
3
-
4by Meredith, Christopher, Herrmann, Ralf, Parry, Cheryl, Liyanage, Khema, Dye, Danielle E., Durling, Hayley J., Duff, Rachael M., Beckman, Kaye, de Visser, Marianne, van der Graaff, Maaike M., Hedera, Peter, Fink, John K., Petty, Elizabeth M., Lamont, Phillipa, Fabian, Vicki, Bridges, Leslie, Voit, Thomas, Mastaglia, Frank L., Laing, Nigel G.Get full text
Published in American journal of human genetics
Article -
5by Straub, Volker, Murphy, Alexander, Udd, Bjarne, Corrado, Angelini, Aymé, Ségolène, Bönneman, Carsten, de Visser, Marianne, Hamosh, Ada, Jacobs, Laura, Khizanishvili, Nina, Kroneman, Madelon, Laflorêt, Pascal, Murphy, Alex, Nigro, Vincenzo, Rufibach, Laura, Sarkozy, Anna, Swanepoel, Shaun, Torrente, Ivan, Udd, Bjarne, Urtizberea, Andoni, Vissing, John, Walter, MaggieGet full text
Published in Neuromuscular disorders : NMD
Article -
6by Mammen, Andrew L., Allenbach, Yves, Stenzel, Werner, Benveniste, Olivier, Allenbach, Yves, Benveniste, Olivier, Bleecker, Jan De, Boyer, Olivier, Casciola-Rosen, Livia, Christopher-Stine, Lisa, Damoiseaux, Jan, Gitiaux, Cyril, Fujimoto, Manabu, Lamb, Janine, Landon-Cardinal, Océane, E. Lundberg, Ingrid, Mammen, Andrew, Nishino, Ichizo, Radke, Josefine, Selva-O'Callaghan, Albert, Stenzel, Werner, Vencovsky, Jiri, de Visser, Marianne, Wang, Guochun, Wedderburn, Lucy, Werth, VictoriaGet full text
Published in Neuromuscular disorders : NMD
Article -
7
-
8
-
9
-
10
-
11by Bolduc, Véronique, Marlow, Gareth, Boycott, Kym M., Saleki, Khalil, Inoue, Hiroshi, Kroon, Johan, Itakura, Mitsuo, Robitaille, Yves, Parent, Lucie, Baas, Frank, Mizuta, Kuniko, Kamata, Nobuyuki, Richard, Isabelle, Linssen, Wim H.J.P., Mahjneh, Ibrahim, de Visser, Marianne, Bashir, Rumaisa, Brais, BernardGet full text
Published in American journal of human genetics
Article -
12by Regardt, Malin, Mecoli, Christopher A, Park, Jin Kyun, de Groot, Ingrid, Sarver, Catherine, Needham, Merrilee, de Visser, Marianne, Shea, Beverly, Bingham, 3rd, Clifton O, Lundberg, Ingrid E, Song, Yeong W, Christopher-Stine, Lisa, Alexanderson, HeleneGet full text
Published in Journal of rheumatology
Article -
13
-
14by De Bleecker, Jan L, De Paepe, Boel, Aronica, Eleonora, de Visser, Marianne, Amato, Anthony, Benveniste, Olivier, De Bleecker, Jan, de Boer, Onno, Dimachkie, Mazen, Gherardi, Romain, Goebel, Hans Hilmar, Hilton-Jones, David, Holton, Janice, Lundberg, Ingrid E, Mammen, Andrew, Mastaglia, Frank, Nishino, Ichizo, Rushing, Elisabeth, Daa Schroder, Henrik, Selcen, Duygu, Stenzel, WernerGet full text
Published in Neuromuscular disorders : NMD
Article -
15by Attarian, Shahram, Young, Peter, Brannagan, Thomas H, Adams, David, Van Damme, Philip, Thomas, Florian P, Casanovas, Carlos, Kafaie, Jafar, Tard, Céline, Walter, Maggie C, Péréon, Yann, Walk, David, Stino, Amro, de Visser, Marianne, Verhamme, Camiel, Amato, Anthony, Carter, Gregory, Magy, Laurent, Statland, Jeffrey M, Felice, KevinGet full text
Published in Orphanet journal of rare diseases
Article -
16
-
17
-
18by Lemmers, Richard J L F, van der Vliet, Patrick J, Granado, David San Leon, van der Stoep, Nienke, Buermans, Henk, van Schendel, Robin, Schimmel, Joost, de Visser, Marianne, van Coster, Rudy, Jeanpierre, Marc, Laforet, Pascal, Upadhyaya, Meena, van Engelen, Baziel, Sacconi, Sabrina, Tawil, Rabi, Voermans, Nicol C, Rogers, Mark, van der Maarel, Silvère MGet full text
Published in Human molecular genetics
Article -
19by Attarian, Shahram, Young, Peter, Brannagan, Thomas H, Adams, David, Van Damme, Philip, Thomas, Florian P, Casanovas, Carlos, Kafaie, Jafar, Tard, Céline, Walter, Maggie C, Péréon, Yann, Walk, David, Stino, Amro, de Visser, Marianne, Verhamme, Camiel, Amato, Anthony, Carter, Gregory, Magy, Laurent, Statland, Jeffrey M, Felice, KevinGet full text
Published in Orphanet journal of rare diseases
Article -
20