Treffer 1 - 20 von 20 für Suche 'Henderson, Christopher JA', Suchdauer: 1,06s Treffer weiter einschränken
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    The GEOTRACES Intermediate Data Product 2014 von Mawji, Edward, Schlitzer, Reiner, Dodas, Elena Masferrer, Abadie, Cyril, Anderson, Robert F., Baars, Oliver, Bakker, Karel, Baskaran, Mark, Bates, Nicholas R., Bluhm, Katrin, Bowie, Andrew, Bown, Johann, Boyle, Edward A., Branellec, Pierre, Brzezinski, Mark A., Bucciarelli, Eva, Buesseler, Ken, Butler, Edward, Cai, Pinghe, Cardinal, Damien, Cheng, Hai, Chever, Fanny, Church, Thomas M., Colman, Albert S., Cutter, Gregory A., de Baar, Hein J.W., Dehairs, Frank, Deng, Feifei, Dieu, Huong Thi, Dulaquais, Gabriel, Echegoyen-Sanz, Yolanda, Lawrence Edwards, R., Fitzsimmons, Jessica, Frank, Martin, Friedrich, Jana, Fripiat, François, Galer, Stephen J.G., Solsona, Ester Garcia, Gerringa, Loes J.A., Godoy, José Marcus, Grossteffan, Emilie, Hatta, Mariko, Hayes, Christopher T., Heller, Maija Iris, Henderson, Gideon, Huang, Kuo-Fang, Jenkins, William J., John, Seth, Kenna, Timothy C., Klunder, Maarten, Kretschmer, Sven, Laan, Patrick, Labatut, Marie, Lam, Phoebe J., Lannuzel, Delphine, Lohan, Maeve C., Masqué, Pere, McClain, Charles R., Measures, Christopher, Middag, Rob, Moffett, James, Navidad, Alicia, Nishioka, Jun, Noble, Abigail, Planchon, Frédéric, Pradoux, Catherine, Puigcorbé, Viena, Quay, Paul, Radic, Amandine, Rehkämper, Mark, Remenyi, Tomas, Rintoul, Stephen, Roeske, Tobias, Rosenberg, Mark, van der Loeff, Michiel Rutgers, Ryabenko, Evgenia, Saito, Mak A., Sarthou, Géraldine, Schauer, Ursula, Scott, Peter, Sedwick, Peter N., Smethie, William, Smith, Geoffrey J., Sohrin, Yoshiki, Speich, Sabrina, Stichel, Torben, Stutsman, Johnny, Swift, James H., Tagliabue, Alessandro, Tsunogai, Urumu, van Weerlee, Evaline, Venchiarutti, Celia, Wake, Bronwyn, Warner, Mark J., Woodward, E. Malcolm S., Wu, Jingfeng, Wyatt, Neil, Xue, Zichen, Zieringer, Moritz, Zimmer, Louise A.

    Veröffentlicht in Marine chemistry

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    SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile von Al-Jawahiri, Reem, Foroutan, Aidin, McConkey, Haley, Levy, Michael, Haghshenas, Sadegheh, Rooney, Kathleen, Turner, Jasmin, Shears, Debbie, Holder, Muriel, Lefroy, Henrietta, Castle, Bruce, Reis, Linda M., Semina, Elena V., Nickerson, Deborah, Bamshad, Michael, Leal, Suzanne, Lachlan, Katherine, Chandler, Kate, Clayton-Smith, Jill, Hug, Franziska Phan, Pitteloud, Nelly, Bartoloni, Lucia, Hoffjan, Sabine, Park, Soo-Mi, Thankamony, Ajay, Lees, Melissa, Wakeling, Emma, Naik, Swati, Hanker, Britta, Girisha, Katta M., Agolini, Emanuele, Giuseppe, Zampino, Alban, Ziegler, Tessarech, Marine, Keren, Boris, Afenjar, Alexandra, Zweier, Christiane, Smol, Thomas, Nobuhiko, Okamoto, Sekiguchi, Futoshi, Tsuchida, Naomi, Matsumoto, Naomichi, Kou, Ikuyo, Yonezawa, Yoshiro, Ikegawa, Shiro, Callewaert, Bert, Ambrose, John C., Arumugam, Prabhu, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R., Brittain, Helen, Caulfield, Mark J., Chan, Georgia C., Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E.A., Leong, Ivonne U.S., Lopez, Javier F., FionaMaleady-Crowe, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C., Odhams, Chris A., Patch, Christine, Perez-Gil, Daniel, Pullinger, John, Rendon, Augusto, TimRogers, Savage, Kevin, Sawant, Kushmita, Scott, Richard H., Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Thompson, Simon R., Tucci, Arianna, Williams, Eleanor, Kleinendorst, Lotte, Donaldson, Alan, Alders, Marielle, De Paepe, Anne, Sadikovic, Bekim, McNeill, Alisdair

    Veröffentlicht in Genetics in medicine

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