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Mismatch repair-deficient crypt foci in Lynch syndrome: molecular alterations and association with clinical parameters by Staffa, Laura (Author) , Echterdiek, Fabian Friedrich (Author) , Nelius, Nina (Author) , Benner, Axel (Author) , Werft, Wiebke (Author) , Lahrmann, Bernd (Author) , Grabe, Niels (Author) , Schneider, Martin (Author) , Tariverdian, Mirjam (Author) , Knebel Doeberitz, Magnus von (Author) , Kloor, Matthias (Author) ,

• Verlag, kostenfrei, Volltext
• Verlag, kostenfrei, Volltext
• Verlag, kostenfrei, Volltext
• Verlag, kostenfrei, Volltext

KIT mutation and loss of 14q may be sufficient for the development of clinically symptomatic very low-risk GIST by Klinke, Olaf (Author) , Mizani, Tuba (Author) , Baldwin, Gouri (Author) , Bancel, Brigitte (Author) , Devouassoux-Shisheboran, Mojgan (Author) , Scoazec, Jean-Yves (Author) , Bringuier, Pierre-Paul (Author) , Feederle, Regina (Author) , Jauch, Anna (Author) , Hinderhofer, Katrin (Author) , Taniere, Philippe (Author) , Delecluse, Henri-Jacques (Author) ,

• Resolving-System, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext