Almost 2% of Spanish breast cancer families are associated to germline pathogenic mutations in the ATM gene by Tavera-Tapia, A., Pérez-Cabornero, L., Macías, J. A., Ceballos, M. I., Roncador, G., de la Hoya, M., Barroso, A., Felipe-Ponce, V., Serrano-Blanch, R., Hinojo, C., Miramar-Gallart, M. D., Urioste, M., Caldés, T., Santillan-Garzón, S., Benitez, J., Osorio, A.

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Incidence of −93 MLH1 promoter polymorphism in familial and sporadic colorectal cancer by Martínez-Urueña, N., Macías, L., Pérez-Cabornero, L., Infante, M., Lastra, E., Cruz, J. J., Miner, C., González, R., Durán, M.

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BRCA1 5272-1G>A and BRCA2 5374delTATG are founder mutations of high relevance for genetic counselling in breast/ovarian cancer families of Spanish origin by Infante, M, Durán, M, Acedo, A, Pérez-Cabornero, L, Sanz, DJ, García-González, M, Beristain, E, Esteban-Cardeñosa, E, De La Hoya, M, Teulé, A, Vega, A, Tejada, M-I, Lastra, E, Miner, C, Velasco, EA

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Lynch syndrome diagnostics: decision-making process for germ-line testing by Lastra, Enrique, García-González, María, Llorente, Beatriz, Bernuy, Coralina, Barrio, M. Jesús, Pérez-Cabornero, Lucía, Durán, Mercedes, García-Girón, Carlos

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Poster session 1 by Schlueter, J., Brand, T., Henderson, D. J., Boczonadi, V., Humbert, P., Chaudhry, B., Sedmera, D., Svatunkova, J., Kockova, R., Sankova, B., Lopez Sanchez, C., Franco, D., Aranega, A., Garcia-Martinez, V., Demina, E., Miroshikova, V., Denisenko, A., Schwarzman, A., Sanchez-Cabo, F., Torroja, C., Benguria, A., Buchan, R., Srivastava, P., Martinez, F., Barton, P., Cook, S., Dopazo, A., Lara-Pezzi, E., Rai, H., Kumar, S., Sharma, A. K., Mastana, S., Kapoor, A., Pandey, C. M., Agrawal, S., Sinha, N., Lipkova, J., Goldbergova, M., Parenica, J., Bienertova Vasku, J., Vasku, A., Kala, P., Spinar, J., Perez-Cabornero, L., Cantalapiedra, D., Forteza, A., Saez-Villaverde, R., Zumalde, J., Fernandez-Pedrosa, V., Zuniga-Trejos, S., Gil-Borja, M., Lazaro, M., Santillan, S., Costa, M., Cortez-Dias, N., Carrilho-Ferreira, P., Silva, D., Jorge, C., Placido, R., Calisto, C., Fiuza, M., Nunes Diogo, A., Enguita, F. J., Sillje, H. H. W., Lu, B., Yu, H., Zwartbol, M., Ruifrok, W. P., Van Gilst, W. H., De Boer, R. A., Zaliaduonyte-Peksiene, D., Simonyte, S., Lesauskaite, V., Vaskelyte, J., Mizariene, V., Zaliunas, R., Tigchelaar, W., Barlaka, E., Lazou, A., Del Giudice, C., Cipolletta, E., Anastasio, A., Santulli, G., Rusciano, M., Maione, A. S., Campiglia, P., Illario, M., Trimarco, B., Iaccarino, G., Frentzou, G. A., Drinkhill, M. J., Turner, N. A., Ball, S. G., Ainscough, J. F. X., Bertrand, L., Mailleux, F., Hammond, J., Ginion, A., Hue, L., Balligand, J. L.

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Incidence of −93 MLH 1 promoter polymorphism in familial and sporadic colorectal cancer by Martínez‐Urueña, N., Macías, L., Pérez‐Cabornero, L., Infante, M., Lastra, E., Cruz, J. J., Miner, C., González, R., Durán, M.

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