Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry

di Vasen, Hans F. A., Velthuizen, Mary E., Kleibeuker, Jan H., Menko, Fred H., Nagengast, Fokke M., Cats, Annemieke, van der Meulen-de Jong, Andrea E., Breuning, Martijn H., Roukema, Anne J., van Leeuwen-Cornelisse, Inge, de Vos tot Nederveen Cappel, Wouter H., Wijnen, Juul T.
Pubblicato in Fam Cancer (2016)

Seven New Mutations in hMSH2, an HNPCC Gene, Identified by Denaturing Gradient-Gel Electrophoresis

di Wijnen, Juul, Vasen, Hans, Khan, P. Meera, Menko, Fred H., van der Klift, Heleen, van Leeuwen, Claus, van den Broek, Marianne, van Leeuwen-Cornelisse, Inge, Nagengast, Fokko, Meijers-Heijboer, Anne, Lindhout, Dick, Griffioen, Gerrit, Cats, Annemieke, Kleibeuker, Jan, Varesco, Liliana, Bertario, Lucio, Bisgaard, Marie Luise, Mohr, Jan, Fodde, Riccardo
Pubblicazione 1995