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    Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling von Snijders Blok, Lot, Madsen, Erik, Juusola, Jane, Gilissen, Christian, Baralle, Diana, Reijnders, Margot R.F., Venselaar, Hanka, Helsmoortel, Céline, Cho, Megan T., Hoischen, Alexander, Vissers, Lisenka E.L.M., Koemans, Tom S., Wissink-Lindhout, Willemijn, Eichler, Evan E., Romano, Corrado, Van Esch, Hilde, Stumpel, Connie, Vreeburg, Maaike, Smeets, Eric, Oberndorff, Karin, van Bon, Bregje W.M., Shaw, Marie, Gecz, Jozef, Haan, Eric, Bienek, Melanie, Jensen, Corinna, Loeys, Bart L., Van Dijck, Anke, Innes, A. Micheil, Racher, Hilary, Vermeer, Sascha, Di Donato, Nataliya, Rump, Andreas, Tatton-Brown, Katrina, Parker, Michael J., Henderson, Alex, Lynch, Sally A., Fryer, Alan, Ross, Alison, Vasudevan, Pradeep, Kini, Usha, Newbury-Ecob, Ruth, Chandler, Kate, Male, Alison, Dijkstra, Sybe, Schieving, Jolanda, Giltay, Jacques, van Gassen, Koen L.I., Schuurs-Hoeijmakers, Janneke, Tan, Perciliz L., Pediaditakis, Igor, Haas, Stefan A., Retterer, Kyle, Reed, Patrick, Monaghan, Kristin G., Haverfield, Eden, Natowicz, Marvin, Myers, Angela, Kruer, Michael C., Stein, Quinn, Strauss, Kevin A., Brigatti, Karlla W., Keating, Katherine, Burton, Barbara K., Kim, Katherine H., Charrow, Joel, Norman, Jennifer, Foster-Barber, Audrey, Kline, Antonie D., Kimball, Amy, Zackai, Elaine, Harr, Margaret, Fox, Joyce, McLaughlin, Julie, Lindstrom, Kristin, Haude, Katrina M., van Roozendaal, Kees, Brunner, Han, Chung, Wendy K., Kooy, R. Frank, Pfundt, Rolph, Kalscheuer, Vera, Mehta, Sarju G., Katsanis, Nicholas, Kleefstra, Tjitske


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    Prognostic significance of MRI-detected extramural venous invasion according to grade and response to neo-adjuvant treatment in locally advanced rectal cancer A national cohort stu... von Geffen, Eline G.M. van, Nederend, Joost, Sluckin, Tania C., Hazen, Sanne-Marije J.A., Aalbers, Arend G.J., van Aalten, Susanna M., Amelung, Femke J., Ashruf, Jesse F., Bakers, Frans C.H., Barendse, Renée M., Beets, Geerard L., Blok, Robin D., van Bockel, Liselotte W., den Boer, Frank C., Boogerd, Leonora S.F., Borstlap, Wernard A.A., Bouwman, Johanna E., Bradshaw, Jennifer, Burger, Jacobus W.A., Cnossen, Jeltsje S., Coebergh van den Braak, Robert R.J., Corver, Maaike, Crolla, Rogier M.P.H., Daniëls-Gooszen, Alette W., Demirkiran, Ahmet, Derksen, Tyche, van Dop, Ilse M., Droogh-de Greve, Kitty E., Dunker, Michalda S., Duyck, Johan, van Duyn, Eino B., van Egdom, Laurentine S.E., Eijlers, Bram, van Erp, Anne C., van Essen, Jeroen A., Fabry, Hans F.J., Feitsma, Eline A., Frietman, Bas, van Geel, Anne M., Govaert, Marc J.P.M., de Haas, Robbert J., den Hartogh, Mariska D., Hogewoning, Cornelis R.C., van der Hul, René L., van Hulst, Rieke, Imani, Farshad, Keizers, Bas, Kortekaas, Robert T.J., Lahuis, Derk H.H., Martens, MilouH, Meijnen, Philip, Muller, Karin, Musters, Gijsbert D., de Nes, Lindsey C.F., Nonner, Joost, Noordman, Bo J., Nordkamp, Stefi, Olthof, Pim B., Oosterling, Steven J., Ootes, Daan, Oppedijk, Vera, Peeters, Koen C.M.J., Pereboom, Ilona T.A., Peringa, Jan, Polat, Fatih, Renger, Rutger-Jan, Rombouts, Anouk J.M., Roskott-ten Brinke, Ellen A., Rouw, Dennis B., Rozema, Tom, Schasfoort, Renske A., Scheurkogel, Merel M., Schuivens, Puck M.E., Slob, Marjan J., van der Sluis, Martsje, Smalbroek, Bo P., Tielbeek, Jeroen A.W., van Tilborg, Fiek, van Trier, Dorothée, van der Valk, Maxime J.M., Vanhooymissen, Inge J.S., Vasbinder, G. Boudewijn C., Velema, Laura A., Verduin, Wouter M., Verhagen, Tim, Verrijssen, An-Sofie E., Vliegen, Roy F.A., Voets, Sophie, de Vries, Marianne, van Vugt, Bas S.T., Wegdam, Johannes A., van Wely, Bob J., Westerterp, Marinke, Woensdregt, Karlijn, van der Wolk, Sander, Zamaray, Bobby, Zandvoort, Herman J.A., Zheng, Kang J., Zimmerman, David D.E., Zorgdrager, Marcel


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    Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling von Snijders Blok, Lot, Madsen, Erik, Juusola, Jane, Gilissen, Christian, Baralle, Diana, Reijnders, Margot R.F, Venselaar, Hanka, Helsmoorte, Céline, Cho, Megan T, Hoischen, Alexander, Vissers, Lisenka E.L.M, Koemans, Tom S, Wissink-Lindhout, Willemijn, Eichler, Evan E, Romano, Corrado, Van Esch, Hilde, Stumpel, Connie, Vreeburg, Maaike, Smeets, Eric, Obemdorff, Karin, van Bon, Bregje W.M, Shaw, Marie, Gecz, Jozef, Haan, Eric, Bienek, Melanie, Jensen, Corinna, Loeys, Bart L, Van Dijck, Anke, Innes, A. Micheil, Racher, Hilary, Vermeer, Sascha, Di Donato, Nataliya, Rump, Andreas, Tatton-Brown, Katrina, Parker, Michael J, Henderson, Alex, Lynch, Sally A, Fryer, Alan, Ross, Alison, Vasudevan, Pradeep, Kini, Usha, Newbury-Ecob, Ruth, Chandler, Kate, Male, Alison, the DDD Study, Dijkstra, Sybe, Schieving, Jolanda, Giltay, Jacques, van Gassen, Koen L.I, Schuurs-Hoeijmakers, Janneke, Tan, Perciliz L, Pediaditakis, Igor, Haas, Stefan A, Retterer, Kyle, Reed, Patrick, Monaghan, Kristin G, Haverfield, Eden, Natowicz, Marvin, Myers, Angela, Kruer, Michael C, Stein, Quinn, Strauss, Kevin A, Brigatti, Karlla W, Keating, Katherine, Burton, Barbara K, Kim, Katherine H, Charrow, Joel, Norman, Jennifer, Foster-Barber, Audrey, Kline, Antonie D, Kimball, Amy, Zackai, Elaine, Harr, Margaret, Fox, Joyce, McLaughlin, Julie, Lindstrom, Kristin, Haude, Katrina M, van Roozendaal, Kees, Brunner, Han, Chung, Wendy K, Kooy, R. Frank, Pfundt, Rolph, Kalscheuer, Vera, Mehta, Sarju G, Katsanis, Nicholas, Kleefstra, Tjitske


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