Treffer 1 - 20 von 56 für Suche 'Schneider, Ana Elizabeth', Suchdauer: 1,58s Treffer weiter einschränken
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    Burden of disease in Brazil, 1990–2016: a systematic subnational analysis for the Global Burden of Disease Study 2016 von Marinho, Fatima, de Azeredo Passos, Valéria Maria, Carvalho Malta, Deborah, Barboza França, Elizabeth, Abreu, Daisy M X, Araújo, Valdelaine E M, Bustamante-Teixeira, Maria Teresa, Camargos, Paulo A M, da Cunha, Carolina Cândida, Duncan, Bruce Bartholow, Felisbino-Mendes, Mariana Santos, Guerra, Maximiliano Ribeiro, Guimaraes, Mark D C, Lotufo, Paulo A, Marcenes, Wagner, Oliveira, Patricia Pereira Vasconcelos, de Moares Pedroso, Marcel, Ribeiro, Antonio L, Schmidt, Maria Inês, Teixeira, Renato Azeredo, Vasconcelos, Ana Maria Nogales, Barreto, Mauricio L, Bensenor, Isabela M, Brant, Luisa C C, Claro, Rafael M, Costa Pereira, Alexandre, Cousin, Ewerton, Curado, Maria Paula, dos Santos, Kadine Priscila Bender, Faro, André, Ferri, Cleusa P, Furtado, João M, Gall, Julia, Glenn, Scott D, Goulart, Alessandra Carvalho, Ishitani, Lenice Harumi, Kieling, Christian, Ladeira, Roberto Marini, Machado, Isis Eloah, Martins, Sheila Cristina Ouriques, Martins-Melo, Francisco Rogerlândio, Melo, Ana Paula Souto, Miller-Petrie, Molly K, Mooney, Meghan D, Nunes, Bruno P, Palone, Marcos Roberto Tovani, Pereira, Claudia C, Rasella, Davide, Ray, Sarah E, Roever, Leonardo, de Freitas Saldanha, Raphael, Santos, Itamar S, Schneider, Ione J C, Santos Silva, Diego Augusto, Silveira, Dayane Gabriele Alves, Soares Filho, Adauto Martins, Moraes Sousa, Tatiane Cristina, Szwarcwald, Celia L, Traebert, Jefferson, Velasquez-Melendez, Gustavo, Wang, Yuan-Pang, Lozano, Rafael, Murray, Christopher J L, Naghavi, Mohsen

    Veröffentlicht in The Lancet (British edition)

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    Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population von Hunter, Jessica E., Riddle, Leslie, Joseph, Galen, Amendola, Laura M., Gilmore, Marian J., Zepp, Jamilyn M., Shuster, Elizabeth, Bulkley, Joanna E., Muessig, Kristin R., Anderson, Katherine P., Goddard, Katrina A.B., Wilfond, Benjamin S., Leo, Michael C., Allen, Jake, Angelo, Frank, Arnold, Briana L., Bellcross, Cecelia, Bendelow, Tiffany, B, Barbara, Biesecker, Breslin, Kristin D., Booker, Kristina F., Caruncho, Mikaella, Davis, James V., Deutsch, Sonia, Devine, Beth, Dorschner, Michael O., Duenas, Devan, Eubanks, Donna J., Feigelson, Heather Spencer, Freed, Amanda S., Greaney, Clay, Gruß, Inga, Guerra, Claudia, Guo, Boya, Holup, Joan, Ingphakorn, Chalinya L., Jackson, Paige, Jarvik, Gail P., Jenkins, Charisma L., Karliner, Leah S., Kaufmann, Tia, Keast, Erin, Knerr, Sarah, Koomas, Alyssa H., Kraft, Stephanie A., Lee, Mi H., Lee, Robin, Soo-Jin Lee, Sandra, Lewis, Hannah S., Liles, Elizabeth G., Lindberg, Nangel M., Lynch, Frances, McMullen, Carmit K., Medina, Elizabeth, Mittendorf, Kathleen F., Muessig, Kristin R., Okuyama, Sonia, Peterson, C. Samuel, Paolucci, Angela R., Perez, Rosse Rodriguez, Porter, Kathryn M., Ransom, Chelese L., Reyes, Ana, Robinson, Sperry, Rolf, Bradley A., Rope, Alan F., Schield, Emily, Schneider, Jennifer L., Shipman, Kelly J., Shirts, Brian H., Shuster, Elizabeth, Syngal, Sapna, Torgrimson-Ojerio, Britta N., Ukaegbu, Chinedu, Vandermeer, Meredith L., Varga, Alexandra M., Veenstra, David L., Whitebirch, W. Chris, Lee White, Larissa

    Veröffentlicht in Genetics in medicine

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    Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access von Amendola, Laura M., Shuster, Elizabeth, Leo, Michael C., Dorschner, Michael O., Rolf, Bradley A., Shirts, Brian H., Gilmore, Marian J., Okuyama, Sonia, Zepp, Jamilyn M., Kauffman, Tia L., Mittendorf, Kathleen F., Bellcross, Cecilia, Jenkins, Charisma L., Joseph, Galen, Riddle, Leslie, Syngal, Sapna, Ukaegbu, Chinedu, Goddard, Katrina A.B., Wilfond, Benjamin S., Jarvik, Gail P., Allen, Jake, Amendola, Laura M., Anderson, Katherine P., Angelo, Frank, Arnold, Briana L., Bellcross, Cecelia, Bendelow, Tiffany, Biesecker, Barbara B., Breslin, Kristin D., Bulkley, Joanna E., Booker, Kristina F., Caruncho, Mikaella, Davis, James V., Deutsch, Sonia, Devine, Beth, Dorschner, Michael O., Duenas, Devan M., Eubanks, Donna J., Feigelson, Heather Spencer, Freed, Amanda S., Gilmore, Marian J., Goddard, Katrina A.B., Greaney, Clay, Gruß, Inga, Guerra, Claudia, Guo, Boya, Holup, Joan, Hunter, Jessica Ezzell, Ingphakorn, Chalinya L., Jackson, Paige, Jarvik, Gail P., Jenkins, Charisma L., Joseph, Galen, Karliner, Leah S., Kauffman, Tia L., Keast, Erin, Knerr, Sarah, Koomas, Alyssa H., Kraft, Stephanie A., Lee, Mi H., Lee, Robin, Soo-Jin Lee, Sandra, Leo, Michael C., Lewis, Hannah S., Liles, Elizabeth G., Lindberg, Nangel M., Lynch, Frances, McMullen, Carmit K., Medina, Elizabeth, Mittendorf, Kathleen F., Muessig, Kristin R., Okuyama, Sonia, Peterson, C. Samuel, Paolucci, Angela R., Perez, Rosse Rodriguez, Porter, Kathryn M., Ransom, Chelese L., Reyes, Ana, Riddle, Leslie S., Robinson, Sperry, Rolf, Bradley A., Rope, Alan F., Schield, Emily, Schneider, Jennifer L., Shipman, Kelly J., Shirts, Brian H., Shuster, Elizabeth, Syngal, Sapna, Torgrimson-Ojerio, Britta N., Ukaegbu, Chinedu, Vandermeer, Meredith L., Varga, Alexandra M., Veenstra, David L., Whitebirch, W. Chris, Lee White, Larissa, Wilfond, Benjamin S., Zepp, Jamilyn M.

    Veröffentlicht in Genetics in medicine

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