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    The role of copy number variants in the genetic architecture of common familial epilepsies von Almanza Fuerte, Edith P., Nguyen, John, Mehaffey, Michelle, Sulovari, Arvis, Wang, Tianyun, Galey, Miranda, Miller, Danny E., Eichler, Evan E., Mefford, Heather C., Abou‐Khalil, Bassel, Afawi, Zaid Afawi, Allen, Andrew S., Amrom, Dina, Andermann, Eva, Bautista, Jocelyn F., Bellows, Susannah T., Berkovic, Samuel F., Bluvstein, Judith, Boro, Alexis, Burgess, Rosemary, Cascino, Gregory D., Chung, Seo‐Kyung, Consalvo, Damian, Cossette, Patrick, Crompton, Douglas E., Crumrine, Patricia, Curtis, Sarah W., Delanty, Norman, Devinsky, Orrin, Dlugos, Dennis, Ellis, Colin A., Epstein, Michael P., Fiol, Miguel, Fountain, Nathan B., Freyer, Catharine, Friedman, Dan, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gravel, Micheline, Haas, Kevin, Harris, Rebekah V., Haut, Sheryl, Heinzen, Erin L., Helmers, Sandra, Henry, Olivia J., Joshi, Sucheta, Kirsch, Heidi E., Kivity, Sara, Knowlton, Robert C., Kossoff, Eric, Kuzniecky, Ruben, Loeb, Rebecca, Lowenstein, Daniel H., Marson, Anthony G., McCormack, Mark, McGuire, Shannon M., McKenna, Kevin, Motika, Paul V., Mullen, Saul A., Novotny, Edward J., O’Brien, Terence J., Oliver, Karen L., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack M., Park, Kristen L., Paterson, Sarah J., Petrovski, Slave, Pickrell, William O., Poduri, Annapurna, Rees, Mark I., Sadleir, Lynette G., Scheffer, Ingrid E., Shellhaas, Renee A., Sherr, Elliott H., Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K., Sirven, Joseph, Smith, Michael C., Smith, Philip E. M., Sperling, Michael R., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Vining, Eileen P. G., Von Allmen, Gretchen K., Weisenberg, Judith, Widdess‐Walsh, Peter, Winawer, Melodie R.

    Veröffentlicht in Epilepsia (Copenhagen)

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    Considerations for reporting variants in novel candidate genes identified during clinical genomic testing von Chong, Jessica X., Berger, Seth I., Baxter, Samantha, Hawley, Megan H., DiTroia, Stephanie, Alvarez, Raquel, Amin, Mutaz, Assimes, Themistocles, Auriga, Light, Bamshad, Mike, Behera, Sairam, Blankenmeister, Benjamin, Blue, Elizabeth, Bonner, Devon, Boone, Philip, Brand, Harrison, Chavez, Clarisa, Chen, Ziwei, Cui, Ya Allen, Currin, Sara, Daber, Robert, Dardas, Zain, Davis, Colleen, Dawood, Moez, Doddapaneni, Harsha, Duong, Nhat, Duyzend, Michael, Eichler, Evan, Emami, Sara, Fraser, Jamie, Fusaro, Vincent, Garcia, Brandon, Garimella, Kiran, Gifford, Casey, Goddard, Page, Gogarten, Stephanie, Gogate, Nikhita, Sousa, Rodrigo Guarischi, Gudmundsson, Sanna, Gulati, Ashima, Hall, Stacey, Harvey, William, Horike-Pyne, Martha, Hu, Jianhong, Saad, Ahmed K., Knoblach, Susan, Ko, Arthur, Kundaje, Anshul, Kundu, Soumya, Larsson, Katie, Lemire, Gabrielle, Li, Yidan, LoTempio, Jonathan, Ma, Jialan, Mahmoud, Medhat, Malani, Nirav, Mangilog, Brian, Martinez, Eva, Mastrorosa, Francesco Kumara, Matalon, Dena, May, Susanne, Meador, Lauren, Mitani, Tadahiro, Montgomery, Stephen, Moyses, Mariana, Munderloh, Chloe, Muzny, Donna, Nykamp, Keith, O'Callaghan, William, Pan, Miao, Panchal, Piyush, Payne, Sheryl, Petrowski, Paul, Porter, Elizabeth, Prosser, Jaime, Quertermous, Thomas, Rai, Archana, Rivera-Munoz, Andres, Sabo, Aniko, Samocha, Kaitlin, Savage, Sarah, Shah, Gulalai, Singh, Mugdha, Smith, Kevin, Smith, Josh, Starita, Lea, Stenton, Sarah, Stilp, Adrienne, Sutton, V. Reid, Tong, Catherine (Cat), Tsao, Philip, Ungar, Rachel, Vilain, Eric, Wei, Chia-Lin, Weisburd, Ben, Wellington, Chris, Westheimer, Emily, Wheeler, Marsha, Wojcik, Monica, Yadav, Rachita

    Veröffentlicht in Genetics in medicine

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