Treffer 1 - 15 von 15 für Suche 'Davis, Devin F.', Suchdauer: 1,99s Treffer weiter einschränken
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7

    Returning integrated genomic risk and clinical recommendations: The eMERGE study von Chisholm, Rex L., Clayton, Ellen Wright, DiVietro, Alanna, Green, Richard, Harden, Maegan V., Limdi, Nita A., Rasmussen, Luke V., Schmidlen, Tara, Cimino, James J., Guiducci, Candace, Harr, Margaret, Larkin, Katie, Mooney, Sean D., Mutai, Brenda, Namjou, Bahram, Perez, Emma F., Saadatagah, Seyedmohammad, Seabolt, Lynn, Shaibi, Gabriel Q., Sharp, Richard R., Sterling, Rene, Tiwari, Hemant K., Allworth, Aimee, DiVietro, Alanna, Khera, Amit, Kontorovich, Amy, Prince, Anya, Iverson, Ayuko, Khales, Bahram Namjou, Benoit, Barbara, Satterfield, Benjamin, Devine, Beth, Grundmeier, Bob, Piening, Brian, Korf, Bruce, Hammack, Catherine, Gascoigne, Caytie, Lange, Christoph, Liu, Cong, Shimbo, Daichi, Singh, Davinder, Edwards, Digna Velez, Morales, Eduardo, Cohn, Elizabeth, Karlson, Elizabeth, DeFranco, Emily, Perez, Emma, Cash, Erin, Berner, Eta, Wang, Fei, Mentch, Frank, Wiesner, Georgia, Belbin, Gillian, Hakonarson, Hakon, Tiwari, Hemant, Thomas, Hope, Hellwege, Jacklyn, Snyder, James, Olson, Janet, Glessner, Joe, Alsip, Jorge, Kannry, Joseph, Peterson, Josh, Galasso, Julia, Starren, Justin, Mittendorf, Kate, Anderson, Katherine, Bonini, Katherine, Rasmussen-Torvik, Laura, Gomez, Lizbeth, Petukhova, Lynn, Beasley, Mark, Horike, Martha, Hamed, Marwan, Davis, Matthew, Preuss, Michael, Shi, Mingjian, Perera, Minoli, Elkind, Mitch, Saadatagah, Mohammad, Netherly, Neil, Lennon, Niall, Limdi, Nita, Robinson, Nora, Elsekaily, Omar, Kovatch, Patricia, O’Reilly, Paul, Murali, Priyanka, Sharp, Richard, Peters, Riki, Rowley, Robb, Freimuth, Robert, Green, Robert, Winter, Robert, Irvin, Ryan, Knerr, Sarah, Bland, S.T., Booth, Stuart James, Desai, Vimi, Luo, Yuan

    Veröffentlicht in Genetics in medicine

    Volltext
    Artikel
  8. 8
  9. 9
  10. 10

    Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11 von Ravenscroft, Thomas A., Fieg, Elizabeth, Zirin, Jonathan, Kanca, Oguz, Adam, Margaret, Agrawal, Pankaj B., Alejandro, Mercedes E., Alvey, Justin, Andrews, Ashley, Azamian, Mahshid S., Bademci, Guney, Balasubramanya, Ashok, Behrens, Edward, Bican, Anna, Bohnsack, John, Botto, Lorenzo, Brown, Gabrielle, Byers, Peter, Chanprasert, Sirisak, Chao, Hsiao-Tuan, Cobban, Laurel A., Cogan, Joy D., Colley, Heather A., Cope, Heidi, Craigen, William J., Crouse, Andrew B., Dai, Hongzheng, Dayal, Jyoti G., Dipple, Katrina, Dorrani, Naghmeh, Draper, David D., Emrick, Lisa T., Falk, Marni, Fernandez, Liliana, Fieg, Elizabeth L., Findley, Laurie C., Gahl, William A., Godfrey, Rena A., Goldman, Alica M., Goldstein, David B., Hamid, Rizwan, Hanchard, Neil A., Hassey, Kelly, Hayes, Nichole, High, Frances, Hing, Anne, Hisama, Fuki M., Holm, Ingrid A., Huang, Yong, Huryn, Laryssa, Isasi, Rosario, Jarvik, Gail P., Jarvik, Jeffrey, Jayadev, Suman, Kiley, Dana, Krasnewich, Donna M., Lam, Christina, Lee, Hane, MacDowall, John, Majcherska, Marta M., Mak, Bryan C., Mamounas, Laura A., Martínez-Agosto, Julian A., McCauley, Jacob, Mulvihill, John J., Newman, John H., Oglesbee, Devin, Pace, Laura, Pallais, J. Carl, Palmer, Christina GS, Posey, Jennifer E., Potocki, Lorraine, Power, Bradley, Pusey, Barbara N., Rives, Lynette, Sacco, Ralph, Sampson, Jacinda B., Samson, Susan L., Scott, C. Ron, Schedl, Timothy, Shashi, Vandana, Tan, Queenie K.-G., Toro, Camilo, Viskochil, Dave, Wahl, Colleen E., Wambach, Jennifer, Wang, Lee-kai, Wener, Mark, Perry, Katherine Wesseling, Westerfield, Monte, Whitlock, Jordan, Yamamoto, Shinya, Yang, John, Yousef, Muhammad, Zastrow, Diane B., Zhao, Chunli, Osmond, Matthew, Postlethwait, John H., Krier, Joel, Bellen, Hugo J.

    Veröffentlicht in Genetics in medicine

    Volltext
    Artikel
  11. 11

    Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases von Krier, Joel B., Züchner, Stephan, Huang, Alden, Bastarache, Lisa, Bican, Anna, Liu, Pengfei, Adam, Margaret, Alejandro, Mercedes E., Alvey, Justin, Azamian, Mahshid S., Bademci, Guney, Baker, Eva, Balasubramanyam, Ashok, Bale, Jim, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bohnsack, John, Bonner, Devon, Boyd, Brenna, Brown, Gabrielle, Burrage, Lindsay C., Butte, Manish J., Coakley, Terra R., Cobban, Laurel A., Cogan, Joy D., Cole, F. Sessions, Cunningham, Michael, Dorrani, Naghmeh, Doss, Argenia L., Douine, Emilie D., Eng, Christine M., Falk, Marni, Ferreira, Carlos, Findley, Laurie C., Fogel, Brent L., Forghani, Irman, Gahl, William A., Glass, Ian, Godfrey, Rena A., Hanchard, Neil A., Hing, Anne, Huryn, Laryssa, Isasi, Rosario, Kiley, Dana, Korrick, Susan, Krakow, Deborah, Lalani, Seema R., LeBlanc, Kimberly, Liu, Xue Zhong, MacDowall, John, MacRae, Calum A., Mamounas, Laura A., Maravilla, Kenneth, Markello, Thomas C., Martin, Beth A., Martin, Martin G., Marwaha, Shruti, McCauley, Jacob, Merritt, J. Lawrence, Might, Matthew, Moretti, Paolo, Murdock, David R., Nakano-Okuno, Mariko, Nickerson, Deborah, Oglesbee, Devin, Pace, Laura, Pallais, J. Carl, Papp, Jeanette C., Phillips, John A., Power, Bradley, Pusey, Barbara N., Raja, Archana N., Renteria, Genecee, Rosenwasser, Natalie, Rossignol, Francis, Ruzhnikov, Maura, Sampson, Jacinda B., Schedl, Timothy, Shin, Jimann, Smith, Edward C., Sun, Angela, Sutton, Shirley, Sweetser, David A., Sybert, Virginia, Toro, Camilo, Tucker, Brianna M., Velinder, Matt, Viskochil, Dave, Wambach, Jennifer, Wang, Lee-kai, Ward, Patricia A., Wener, Mark, Westerfield, Monte, Whitlock, Jordan, Woods, Jeremy D., Yamamoto, Shinya, Yang, John, Zein, Wadih

    Veröffentlicht in Genetics in medicine

    Volltext
    Artikel
  12. 12
  13. 13
  14. 14
  15. 15