Treffer 1 - 20 von 47 für Suche 'Law, Nicholas John Joseph', Suchdauer: 1,40s Treffer weiter einschränken
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    Near-resonance in a System of Sub-Neptunes from TESS von Quinn, Samuel N., Becker, Juliette C., Rodriguez, Joseph E., Hadden, Sam, Huang, Chelsea X., Morton, Timothy D., Adams, Fred C., Armstrong, David, Eastman, Jason D., Horner, Jonathan, Kane, Stephen R., Lissauer, Jack J., Twicken, Joseph D., Vanderburg, Andrew, Wittenmyer, Rob, Ricker, George R., Vanderspek, Roland K., Latham, David W., Seager, Sara, Winn, Joshua N., Jenkins, Jon M., Agol, Eric, Barkaoui, Khalid, Beichman, Charles A., Bouchy, François, Bouma, L. G., Burdanov, Artem, Campbell, Jennifer, Carlino, Roberto, Cartwright, Scott M., Charbonneau, David, Christiansen, Jessie L., Ciardi, David, Collins, Karen A., Collins, Kevin I., Conti, Dennis M., Crossfield, Ian J. M., Daylan, Tansu, Dittmann, Jason, Doty, John, Dragomir, Diana, Ducrot, Elsa, Gillon, Michael, Glidden, Ana, Goeke, Robert F., Gonzales, Erica J., He miniak, Krzysztof G., Horch, Elliott P., Howell, Steve B., Jehin, Emmanuel, Jensen, Eric L. N., Kielkopf, John F., Kristiansen, Martti H., Law, Nicholas, Mann, Andrew W., Marmier, Maxime, Matson, Rachel A., Matthews, Elisabeth, Mazeh, Tsevi, Mori, Mayuko, Murgas, Felipe, Murray, Catriona, Narita, Norio, Nielsen, Louise D., Ottoni, Gaël, Palle, Enric, Paw aszek, Rafa, Pepe, Francesco, de Leon, Jerome Pitogo, Pozuelos, Francisco J., Relles, Howard M., Schlieder, Joshua E., Sebastian, Daniel, Ségransan, Damien, Shporer, Avi, Stassun, Keivan G., Tamura, Motohide, Udry, Stéphane, Waite, Ian, Winters, Jennifer G., Ziegler, Carl

    Veröffentlicht in The Astronomical journal

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    Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome von Shaw, Natalie D, Brand, Harrison, Kupchinsky, Zachary A, Bengani, Hemant, Plummer, Lacey, Jones, Takako I, Erdin, Serkan, Williamson, Kathleen A, Rainger, Joe, Stortchevoi, Alexei, Samocha, Kaitlin, Currall, Benjamin B, Dunican, Donncha S, Collins, Ryan L, Willer, Jason R, Lek, Angela, Lek, Monkol, Nassan, Malik, Pereira, Shahrin, Kammin, Tammy, Lucente, Diane, Silva, Alexandra, Seabra, Catarina M, Chiang, Colby, An, Yu, Ansari, Morad, Rainger, Jacqueline K, Joss, Shelagh, Smith, Jill Clayton, Lippincott, Margaret F, Singh, Sylvia S, Patel, Nirav, Jing, Jenny W, Law, Jennifer R, Ferraro, Nalton, Verloes, Alain, Rauch, Anita, Steindl, Katharina, Zweier, Markus, Scheer, Ianina, Sato, Daisuke, Okamoto, Nobuhiko, Jacobsen, Christina, Tryggestad, Jeanie, Chernausek, Steven, Schimmenti, Lisa A, Brasseur, Benjamin, Cesaretti, Claudia, García-Ortiz, Jose E, Buitrago, Tatiana Pineda, Silva, Orlando Perez, Hoffman, Jodi D, Mühlbauer, Wolfgang, Ruprecht, Klaus W, Loeys, Bart L, Shino, Masato, Kaindl, Angela M, Cho, Chie-Hee, Morton, Cynthia C, Meehan, Richard R, van Heyningen, Veronica, Liao, Eric C, Balasubramanian, Ravikumar, Hall, Janet E, Seminara, Stephanie B, Macarthur, Daniel, Moore, Steven A, Yoshiura, Koh-Ichiro, Gusella, James F, Marsh, Joseph A, Graham, Jr, John M, Lin, Angela E, Katsanis, Nicholas, Jones, Peter L, Crowley, Jr, William F, Davis, Erica E, FitzPatrick, David R, Talkowski, Michael E

    Veröffentlicht in Nature genetics

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    Correction: Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome von Shaw, Natalie D, Brand, Harrison, Kupchinsky, Zachary A, Bengani, Hemant, Plummer, Lacey, Jones, Takako I, Erdin, Serkan, Williamson, Kathleen A, Rainger, Joe, Stortchevoi, Alexei, Samocha, Kaitlin, Currall, Benjamin B, Dunican, Donncha S, Collins, Ryan L, Willer, Jason R, Lek, Angela, Lek, Monkol, Nassan, Malik, Pereira, Shahrin, Kammin, Tammy, Lucente, Diane, Silva, Alexandra, Seabra, Catarina M, Chiang, Colby, An, Yu, Ansari, Morad, Rainger, Jacqueline K, Joss, Shelagh, Smith, Jill Clayton, Lippincott, Margaret F, Singh, Sylvia S, Patel, Nirav, Jing, Jenny W, Law, Jennifer R, Ferraro, Nalton, Verloes, Alain, Rauch, Anita, Steindl, Katharina, Zweier, Markus, Scheer, Ianina, Sato, Daisuke, Okamoto, Nobuhiko, Jacobsen, Christina, Tryggestad, Jeanie, Chernausek, Steven, Schimmenti, Lisa A, Brasseur, Benjamin, Cesaretti, Claudia, García-Ortiz, Jose E, Buitrago, Tatiana Pineda, Silva, Orlando Perez, Hoffman, Jodi D, Mühlbauer, Wolfgang, Ruprecht, Klaus W, Loeys, Bart L, Shino, Masato, Kaindl, Angela M, Cho, Chie-Hee, Morton, Cynthia C, Meehan, Richard R, van Heyningen, Veronica, Liao, Eric C, Balasubramanian, Ravikumar, Hall, Janet E, Seminara, Stephanie B, Macarthur, Daniel, Moore, Steven A, Yoshiura, Koh-ichiro, Gusella, James F, Marsh, Joseph A, Graham, John M, Lin, Angela E, Katsanis, Nicholas, Jones, Peter L, Crowley, William F, Davis, Erica E, FitzPatrick, David R, Talkowski, Michael E

    Veröffentlicht in Nature genetics

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