Treffer 1 - 12 von 12 für Suche 'Alejandra Pinero, Tamara', Suchdauer: 2,18s Treffer weiter einschränken
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    Analysis in the Prospective Lynch Syndrome Database identifies sarcoma as part of the Lynch syndrome tumor spectrum von Dominguez‐Valentin, Mev, Sampson, Julian R., Møller, Pål, Seppälä, Toni T., Plazzer, John‐Paul, Nakken, Sigve, Engel, Christoph, Aretz, Stefan, Jenkins, Mark A., Sunde, Lone, Bernstein, Inge, Capella, Gabriel, Balaguer, Francesc, Thomas, Huw, Evans, D. Gareth, Burn, John, Greenblatt, Marc, Hovig, Eivind, Nielsen, Maartje, Vos tot Nederveen Cappel, Wouter H., Sijmons, Rolf H., Bertario, Lucio, Tibiletti, Maria Grazia, Cavestro, Giulia Martina, Lindblom, Annika, Valle, Adriana Della, Lopez‐Köstner, Francisco, Gluck, Nathan, Katz, Lior H., Heinimann, Karl, Vaccaro, Carlos A., Büttner, Reinhard, Görgens, Heike, Holinski‐Feder, Elke, Morak, Monika, Holzapfel, Stefanie, Hüneburg, Robert, Knebel Doeberitz, Magnus, Loeffler, Markus, Rahner, Nils, Weitz, Jürgen, Steinke‐Lange, Verena, Broeke, Sanne W., Schmiegel, Wolff, Vangala, Deepak, Pylvänäinen, Kirsi, Renkonen‐Sinisalo, Laura, Hopper, John L., Win, Aung Ko, Haile, Robert W., Lindor, Noralane M., Gallinger, Steven, Le Marchand, Loïc, Newcomb, Polly A., Figueiredo, Jane C., Thibodeau, Stephen N., Jensen, Lars Henrik, Madsen, Majbritt Busk, Krøldrup, Lone, Nilbert, Mef, Moreira, Leticia, Sánchez, Ariadna, Serra‐Burriel, Miquel, Pineda, Marta, Navarro, Matilde, Vidal, Joan Brunet, Blanco, Ignacio, Green, Kate, Lalloo, Fiona, Crosbie, Emma J., Hill, James, Denton, Oliver G., Rødland, Einar Andreas, Vasen, Hans, Mints, Miriam, Neffa, Florencia, Esperon, Patricia, Alvarez, Karin, Kariv, Revital, Rosner, Guy, Pinero, Tamara Alejandra, Gonzalez, María Laura, Kalfayan, Pablo, Tjandra, Douglas, Winship, Ingrid M., Macrae, Finlay, Möslein, Gabriela, Mecklin, Jukka‐Pekka

    Veröffentlicht in International journal of cancer

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    Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (vol 22, pg 15, 2020) von Dominguez-Valentin, Mev, Sampson, Julian R., Seppala, Toni T., ten Broeke, Sanne W., Plazzer, John-Paul, Nakken, Sigve, Engel, Christoph, Aretz, Stefan, Jenkins, Mark A., Sunde, Lone, Bernstein, Inge, Capella, Gabriel, Balaguer, Francesc, Thomas, Huw, Evans, D. Gareth, Burn, John, Greenblatt, Marc, Hovig, Eivind, de Vos tot Nederveen Cappel, Wouter H., Sijmons, Rolf H., Bertario, Lucio, Tibiletti, Maria Grazia, Cavestro, Giulia Martina, Lindblom, Annika, Della Valle, Adriana, Lopez-Kostner, Francisco, Gluck, Nathan, Katz, Lior H., Heinimann, Karl, Vaccaro, Carlos A., Buttner, Reinhard, Gorgens, Heike, Holinski-Feder, Elke, Morak, Monika, Holzapfel, Stefanie, Huneburg, Robert, Knebel Doeberitz, Magnus von, Loeffler, Markus, Rahner, Nils, Schackert, Hans K., Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak, Pylvanainen, Kirsi, Renkonen-Sinisalo, Laura, Hopper, John L., Win, Aung Ko, Haile, Robert W., Lindor, Noralane M., Gallinger, Steven, Le Marchand, Loic, Newcomb, Polly A., Figueiredo, Jane C., Thibodeau, Stephen N., Wadt, Karin, Therkildsen, Christina, Okkels, Henrik, Ketabi, Zohreh, Moreira, Leticia, Sanchez, Ariadna, Serra-Burriel, Miquel, Pineda, Marta, Navarro, Matilde, Blanco, Ignacio, Green, Kate, Lalloo, Fiona, Crosbie, Emma J., Hill, James, Denton, Oliver G., Frayling, Ian M., Rodland, Einar Andreas, Vasen, Hans, Mints, Miriam, Neffa, Florencia, Esperon, Patricia, Alvarez, Karin, Kariv, Revital, Rosner, Guy, Pinero, Tamara Alejandra, Gonzalez, Maria Laura, Kalfayan, Pablo, Tjandra, Douglas, Winship, Ingrid M., Macrae, Finlay, Moslein, Gabriela, Mecklin, Jukka-Pekka, Nielsen, Maartje, Moller, Pal

    Veröffentlicht in GENETICS IN MEDICINE

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    Cancer risks by gene, age, and gender in 6350 carriers ofpathogenic mismatch repair variants: findings from the Prospective Lynch SyndromeDatabase von Dominguez-Valentin Mev, Sampson, Julian R, Seppälä, Toni T, ten Broeke Sanne W, John-Paul, Plazzer, Nakken Sigve, Engel, Christoph, Aretz, Stefan, Jenkins, Mark A, Sunde Lone, Bernstein, Inge, Capella, Gabriel, Balaguer Francesc, Thomas, Huw, Gareth, Evans D, Burn, John, Greenblatt, Marc, Hovig Eivind, de Vos tot Nederveen Cappel Wouter H, Sijmons, Rolf H, Bertario Lucio, Tibiletti, Maria Grazia, Cavestro Giulia Martina, Lindblom Annika, Della Valle Adriana, Lopez-Köstner, Francisco, Gluck, Nathan, Katz, Lior H, Heinimann Karl, Vaccaro, Carlos A, Büttner Reinhard, Görgens Heike, Holinski-Feder Elke, Morak Monika, Holzapfel, Stefanie, Hüneburg, Robert, Knebel Doeberitz Magnus von, Loeffler, Markus, Rahner Nils, Schackert, Hans K, Steinke-Lange, Verena, Wolff, Schmiegel, Vangala Deepak, Pylvänäinen Kirsi, Renkonen-Sinisalo Laura, Hopper, John L, Win Aung Ko, Haile, Robert W, Lindor Noralane M, Gallinger, Steven, Le Marchand Loïc, Newcomb, Polly A, Figueiredo, Jane C, Thibodeau, Stephen N, Wadt Karin, Therkildsen, Christina, Okkels Henrik, Ketabi Zohreh, Moreira, Leticia, Sánchez Ariadna, Serra-Burriel Miquel, Pineda, Marta, Navarro, Matilde, Blanco, Ignacio, Green, Kate, Lalloo Fiona, Crosbie, Emma J, Hill, James, Denton, Oliver G, Frayling Ian M, Rødland, Einar Andreas, Vasen Hans, Mints Miriam, Neffa Florencia, Esperon, Patricia, Alvarez, Karin, Kariv Revital, Rosner, Guy, Pinero, Tamara Alejandra, Gonzalez, María Laura, Kalfayan Pablo, Tjandra, Douglas, Winship, Ingrid M, Macrae Finlay, Möslein Gabriela, Jukka-Pekka, Mecklin, Nielsen Maartje, Møller Pål

    Veröffentlicht in Genetics in medicine

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