The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC)

Por Kruger, S, Bier, A, Engel, C, Mangold, E, Pagenstecher, C, von Knebel, Doeber... M, Holinski-Feder, E, Moeslein, G, Schulmann, K, Plaschke, J, Ruschoff, J, Schackert, H, the, G
Publicado em 2005

LKB1 exonic and whole gene deletions are a common cause of Peutz‐Jeghers syndrome

Por Volikos, E, Robinson, J, Aittomäki, K, Mecklin, J‐P, Järvinen, H, Westerman, A M, de Rooij, F W M, Vogel, T, Moeslein, G, Launonen, V, Tomlinson, I P M, Silver, A R J
Publicado em 2006

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz–Jeghers syndrome

Por Alhopuro, P, Katajisto, P, Lehtonen, R, Ylisaukko-oja, S K, Näätsaari, L, Karhu, A, Westerman, A M, Wilson, J H P, de Rooij, F W M, Vogel, T, Moeslein, G, Tomlinson, I P, Aaltonen, L A, Mäkelä, T P, Launonen, V
Publicado em 2005

Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States

Por Kurzawski, G, Suchy, J, Kladny, J, Safranow, K, Jakubowska, A, Elsakov, P, Kucinskas, V, Gardovski, J, Irmejs, A, Sibul, H, Huzarski, T, Byrski, T, Debniak, T, Cybulski, C, Gronwald, J, Oszurek, O, Clark, J, Gozdz, S, Niepsuj, S, Slomski, R, Plawski, A, Lacka-Wojciechows..., A, Rozmiarek, A, Fiszer-Maliszewsk..., L, Bebenek, M, Sorokin, D, Stawicka, M, Godlewski, D, Richter, P, Brozek, I, Wysocka, B, Jawien, A, Banaszkiewicz, Z, Kowalczyk, J, Czudowska, D, Goretzki, P, Moeslein, G, Lubinski, J
Publicado em 2002