Treffer 1 - 20 von 27 für Suche 'McFarland, Janet C.', Suchdauer: 1,17s Treffer weiter einschränken
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    Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy von Spielmann, Nadine, Miller, Gregor, Oprea, Tudor I, Hsu, Chih-Wei, Fobo, Gisela, Frishman, Goar, Montrone, Corinna, Haseli Mashhadi, Hamed, Mason, Jeremy, Munoz Fuentes, Violeta, Leuchtenberger, Stefanie, Ruepp, Andreas, Wagner, Matias, Westphal, Dominik S, Wolf, Cordula, Görlach, Agnes, Sanz-Moreno, Adrián, Cho, Yi-Li, Teperino, Raffaele, Brandmaier, Stefan, Sharma, Sapna, Galter, Isabella Rikarda, Östereicher, Manuela A, Zapf, Lilly, Mayer-Kuckuk, Philipp, Rozman, Jan, Teboul, Lydia, Bunton-Stasyshyn, Rosie K A, Cater, Heather, Stewart, Michelle, Christou, Skevoulla, Westerberg, Henrik, Willett, Amelia M, Wotton, Janine M, Roper, Willson B, Christiansen, Audrey E, Ward, Christopher S, Heaney, Jason D, Reynolds, Corey L, Prochazka, Jan, Bower, Lynette, Clary, David, Selloum, Mohammed, Bou About, Ghina, Wendling, Olivia, Jacobs, Hugues, Leblanc, Sophie, Meziane, Hamid, Sorg, Tania, Audain, Enrique, Gilly, Arthur, Rayner, Nigel W, Hitz, Marc-Phillip, Zeggini, Eleftheria, Wolf, Eckhard, Sedlacek, Radislav, Murray, Steven A, Svenson, Karen L, Braun, Robert E, White, Jaqueline K, Kelsey, Lois, Gao, Xiang, Shiroishi, Toshihiko, Xu, Ying, Seong, Je Kyung, Mammano, Fabio, Tocchini-Valentini, Glauco P, Beaudet, Arthur L, Meehan, Terrence F, Parkinson, Helen, Smedley, Damian, Mallon, Ann-Marie, Wells, Sara E, Grallert, Harald, Wurst, Wolfgang, Marschall, Susan, Fuchs, Helmut, Brown, Steve D M, Flenniken, Ann M, Nutter, Lauryl M J, McKerlie, Colin, Herault, Yann, Lloyd, K C Kent, Dickinson, Mary E, Gailus-Durner, Valerie, Hrabe de Angelis, Martin

    Veröffentlicht in Nature Cardiovascular Research

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    Biallelic Mutations in ATP5F1D , which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder von Oláhová, Monika, Yoon, Wan Hee, Jangam, Sharayu, Fernandez, Liliana, Davidson, Jean M., Grove, Megan E., Fisk, Dianna G., Kohler, Jennefer N., Holmes, Matthew, Huang, Yong, Contrepois, Kévin, Waggott, Daryl, Kim, Young-Mo, Heyman, Heino M., Stratton, Kelly G., Snyder, Michael, Fisher, Paul G., Feichtinger, René G., Mayr, Johannes A., Hall, Julie, Simpson, Michael A., Morris, Andrew A., Schelley, Susan, Friederich, Marisa W., McFarland, Robert, Van Hove, Johan L. K., Yamamoto, Shinya, Wangler, Michael F., Taylor, Robert W., Bernstein, Jonathan A., Adams, David R., Alejandro, Mercedes E., Bacino, Carlos A., Batzli, Gabriel F., Beggs, Alan H., Behnam, Babak, Bican, Anna, Birch, Camille L., Bonner, Devon, Boone, Braden E., Brush, Matthew, Burrage, Lindsay C., Cooper, Cynthia M., D’Souza, Precilla, Dipple, Katrina M., Donnell-Fink, Laurel A., Dorrani, Naghmeh, Dorset, Daniel C., Draper, David D., Eng, Christine M., Ferreira, Carlos, Fogel, Brent L., Friedman, Noah D., Gahl, William A., Glanton, Emily, Gould, Sarah E., Gourdine, Jean-Philippe F., Groden, Catherine A., Gropman, Andrea L., Hanchard, Neil A., Herzog, Matthew R., Jain, Mahim, Kohane, Isaac S., Krieg, Elizabeth L., Krier, Joel B., Lee, Brendan H., Lee, Hane, Levy, Shawn E., Lewis, Richard A., Loo, Sandra K., Loscalzo, Joseph, MacRae, Calum A., Maduro, Valerie V., Majcherska, Marta M., Manolio, Teri A., Marwaha, Shruti, May, Thomas, McCray, Alexa T., Might, Matthew, Moretti, Paolo M., Morimoto, Marie, Nelson, Stan F., Newberry, J. Scott, Novacic, Donna, Pallais, J. Carl, Palmer, Christina G. S., Parker, Neil H., Phillips, John A., Rodan, Lance H., Rosenfeld, Jill A., Sampson, Jacinda B., Samson, Susan L., Schoch, Kelly, Sharma, Prashant, Stoler, Joan M., Stong, Nicholas, Sullivan, Jennifer A., Vogel, Tiphanie P., Walley, Nicole M., Walsh, Chris A.


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    A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing von Zastrow, Diane B., Bonner, Devon, Reuter, Chloe M., Fisk, Dianna G., Yang, Yaping, Eng, Christine M., Fisher, Paul G., Merker, Jason, Schelley, Susan, Zappala, Zach, Prybol, Cameron, Olahova, Monika, Allard, Patrick, Bacino, Carlos A., Beggs, Alan H., Behnam, Babak, Bick, David P., Birch, Camille L., Bostwick, Bret L., Brokamp, Elly, Brown, Donna M., Chen, Shan, Coakley, Terra R., Cogan, Joy D., Cope, Heidi, Craigen, William J., Dayal, Jyoti G., Dell'Angelica, Esteban C., Dipple, Katrina M., Dorrani, Naghmeh, Draper, David D., Dries, Annika M., Eckstein, David J., Emrick, Lisa T., Enns, Gregory M., Esteves, Cecilia, Estwick, Tyra, Ferreira, Carlos, Fieg, Elizabeth L., Fogel, Brent L., Godfrey, Rena A., Goldstein, David B., Hamid, Rizwan, Holm, Ingrid A., Howerton, Ellen M., Huang, Yong, Jones, Angela L., Karaviti, Lefkothea, Krasnewich, Donna M., Korrick, Susan, Koziura, Mary, Krier, Joel B., Kyle, Jennifer E., Lau, C. Christopher, Lazar, Jozef, LeBlanc, Kimberly, Lee, Hane, Lewis, Richard A., Lincoln, Sharyn A., Loo, Sandra K., Malicdan, May Christine V., Mamounas, Laura A., Markello, Thomas C., Martin, Martin G., Martínez‐Agosto, Julian A., May, Thomas, McConkie‐Rosell, Allyn, McCray, Alexa T., Merker, Jason D., Metz, Thomas O., Moretti, Paolo M., Mulvihill, John J., Muzny, Donna M., Nelson, Stan F., Newberry, J. Scott, Nicholas, Sarah K., Orengo, James P., Pallais, J. Carl, Papp, Jeanette C., Phillips, John A., Posey, Jennifer E., Postlethwait, John H., Rosenfeld, Jill A., Sampson, Jacinda B., Shakachite, Lisa, Sharma, Prashant, Stoler, Joan M., Sweetser, David A., Toro, Camilo, Tran, Alyssa A., Urv, Tiina K., Vilain, Eric, Vogel, Tiphanie P., Wahl, Colleen E., Walker, Melissa, Webb‐Robertson, Bobbie‐Jo M., Westerfield, Monte, Wolfe, Lynne A., Yu, Guoyun, Zheng, Allison

    Veröffentlicht in Journal of genetic counseling

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