Treffer 1 - 20 von 20 für Suche 'D Ketabi', Suchdauer: 1,56s Treffer weiter einschränken
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5

    Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report von Dominguez-Valentin, Mev, Crosbie, Emma J., Engel, Christoph, Aretz, Stefan, Macrae, Finlay, Winship, Ingrid, Capella, Gabriel, Thomas, Huw, Nakken, Sigve, Hovig, Eivind, Nielsen, Maartje, Sijmons, Rolf H., Bertario, Lucio, Bonanni, Bernardo, Tibiletti, Maria Grazia, Cavestro, Giulia Martina, Mints, Miriam, Gluck, Nathan, Katz, Lior, Heinimann, Karl, Vaccaro, Carlos A., Green, Kate, Lalloo, Fiona, Hill, James, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Strauß, Hans-Georg, Tecklenburg, Johanna, Holinski-Feder, Elke, Steinke-Lange, Verena, Mecklin, Jukka-Pekka, Plazzer, John-Paul, Pineda, Marta, Navarro, Matilde, Vidal, Joan Brunet, Kariv, Revital, Rosner, Guy, Piñero, Tamara Alejandra, Gonzalez, María Laura, Kalfayan, Pablo, Ryan, Neil, ten Broeke, Sanne W., Jenkins, Mark A., Sunde, Lone, Bernstein, Inge, Burn, John, Greenblatt, Marc, de Vos tot Nederveen Cappel, Wouter H., Della Valle, Adriana, Lopez-Koestner, Francisco, Alvarez, Karin, Büttner, Reinhard, Görgens, Heike, Morak, Monika, Holzapfel, Stefanie, Hüneburg, Robert, von Knebel Doeberitz, Magnus, Loeffler, Markus, Rahner, Nils, Weitz, Jürgen, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, Anna, Auranen, Annika, 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., Therkildsen, Christina, Okkels, Henrik, Ketabi, Zohreh, Denton, Oliver G., Rødland, Einar Andreas, Vasen, Hans, Neffa, Florencia, Esperon, Patricia, Tjandra, Douglas, Möslein, Gabriela, Sampson, Julian R., Evans, D. Gareth, Seppälä, Toni T., Møller, Pål

    Veröffentlicht in Genetics in medicine

    Volltext
    Artikel
  6. 6

    Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report von Seppälä, Toni T., Dominguez-Valentin, Mev, Crosbie, Emma J., Engel, Christoph, Aretz, Stefan, Macrae, Finlay, Winship, Ingrid, Capella, Gabriel, Thomas, Huw, Hovig, Eivind, Nielsen, Maartje, Sijmons, Rolf H., Bertario, Lucio, Bonanni, Bernardo, Tibiletti, Maria G., Cavestro, Giulia M., Mints, Miriam, Gluck, Nathan, Katz, Lior, Heinimann, Karl, Vaccaro, Carlos A., Green, Kate, Lalloo, Fiona, Hill, James, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Strauß, Hans-Georg, Tecklenburg, Johanna, Holinski-Feder, Elke, Steinke-Lange, Verena, Mecklin, Jukka-Pekka, Plazzer, John-Paul, Pineda, Marta, Navarro, Matilde, Vida, Joan B., Kariv, Revital, Rosner, Guy, Piñero, Tamara A., Pavicic, Walter, Kalfayan, Pablo, ten Broeke, Sanne W., Jenkins, Mark A., Sunde, Lone, Bernstein, Inge, Burn, John, Greenblatt, Marc, de Vos tot Nederveen Cappel, Wouter H., Della Valle, Adriana, Lopez-Koestner, Francisco, Alvarez, Karin, Büttner, Reinhard, Görgens, Heike, Morak, Monika, Holzapfel, Stefanie, Hüneburg, Robert, von Knebel Doeberitz, Magnus, Loeffler, Markus, Redler, Silke, Weitz, Jürgen, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, Anna, Hopper, John L., Win, Aung K., Lindor, Noralane M., Gallinger, Steven, Le Marchand, Loïc, Newcomb, Polly A., Figueiredo, Jane C., Thibodeau, Stephen N., Therkildsen, Christina, Wadt, Karin A.W., Mourits, Marian J.E., Ketabi, Zohreh, Denton, Oliver G., Rødland, Einar A., Vasen, Hans, Neffa, Florencia, Esperon, Patricia, Tjandra, Douglas, Möslein, Gabriela, Rokkones, Erik, Sampson, Julian R., Evans, D.G., Møller, Pål


    Volltext
    Artikel
  7. 7
  8. 8
  9. 9
  10. 10
  11. 11
  12. 12
  13. 13
  14. 14

    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

    Volltext
    Artikel
  15. 15
  16. 16
  17. 17
  18. 18
  19. 19
  20. 20