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    Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing von Sifrim, Alejandro, Hitz, Marc-Phillip, Wilsdon, Anna, Breckpot, Jeroen, Turki, Saeed H. Al, Thienpont, Bernard, McRae, Jeremy, Fitzgerald, Tomas W, Singh, Tarjinder, Swaminathan, Ganesh Jawahar, Prigmore, Elena, Rajan, Diana, Abdul-Khaliq, Hashim, Banka, Siddharth, Bauer, Ulrike M.M, Bentham, Jamie, Berger, Felix, Bhattacharya, Shoumo, Bu'Lock, Frances, Canham, Natalie, Colgiu, Irina-Gabriela, Cosgrove, Catherine, Cox, Helen, Daehnert, Ingo, Daly, Allan, Danesh, John, Fryer, Alan, Gewillig, Marc, Hobson, Emma, Hoff, Kirstin, Homfray, Tessa, the INTERVAL Study, Kahlert, Anne-Karin, Ketley, Ami, Kramer, Hans-Heiner, Lachlan, Katherine, Lampe, Anne Katrin, Louw, Jacoba J, Manickara, Ashok Kumar, Manase, Dorin, McCarthy, Karen P, Metcalfe, Kay, Moore, Carmel, Newbury-Ecob, Ruth, Omer, Seham Osman, Ouwehand, Willem H, Park, Soo-Mi, Parker, Michael J, Pickardt, Thomas, Pollard, Martin O, Robert, Leema, Roberts, David J, Sambrook, Jennifer, Setchfield, Kerry, Stiller, Brigitte, Thornborough, Chris, Toka, Okan, Watkins, Hugh, Williams, Denise, Wright, Michael, Mital, Seema, Daubeney, Piers E.F, Keavney, Bernard, Goodship, Judith, the UK10K Consortium, Abu-Sulaiman, Riyadh Mahdi, Klaassen, Sabine, Wright, Caroline F, Firth, Helen V, Barrett, Jeffrey C, Devriendt, Koenraad, FitzPatrick, David R, Brook, J. David, the Deciphering Developmental Disorders Study, Hurles, Matthew E

    Veröffentlicht in Nature Genetics

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    Testing a global standard for quantifying species recovery and assessing conservation impact von Akçakaya, H Resit, Bennett, Elizabeth L, Brooks, Thomas M, Heath, Anna, Hedges, Simon, Hilton-Taylor, Craig, Hoffmann, Michael, Hochkirch, Axel, Jenkins, Richard, Long, Barney, Mallon, David P, Milner-Gulland, EJ, Stuart, Simon N, Young, Richard P, Arbetman, Marina, Bacchetta, Gianluigi, Badola, Ruchi, Bino, Gilad, Borges, Paulo AV, Boughton, Raoul K, Camacho-Badani, Teresa, Carmichael, Ruth H, Carrero, Christina, Carroll, John P, Catsadorakis, Giorgos, Chapron, Guillaume, Chowdhury, Gawsia Wahidunnessa, Cogoni, Donatella, Constantine, Rochelle, Daltry, Jennifer C, Das, Goura Chandra, Davey, Alexandra, Fernandes, Fernando Moreira, Fernandez, Eduardo Pinheiro, Finucci, Brittany, Földesi, Rita, Forstner, Michael RJ, Garcia-Sandoval, Ricardo, Gatan-Balbas, Marites, González, Benito A, Grant, Tandora D, van Grunsven, Roy HA, Gryzenhout, Marieka, Hagen, Christian A, Hall, Madison B, Hallerman, Eric, Hare, Kelly, Hartdegen, Ruston, Hatfield, Richard, Hussain, Syed Ainul, Jacques, Hélène, Katdare, Suyash, Kaunda-Arara, Boaz, Louis, Edward, Loy, Anna, Lughadha, Eimear Nic, Mangel, Jeffrey C, Martin, Gabriel M, Martinelli, Gustavo, McGowan, Philip JK, McInnes, Alistair, Millard, Michael J, Nguyen, Anh Ha, Nordmeyer, Cale, Norris, Darren, O'Brien, Mark, Oda, Gabriela Akemi, Outerbridge, Mark Evan, Pérez-Jiménez, Juan Carlos, Portela, Rita de Cassia Quitete, Prohaska, Ana, Quintana, Manuel G, Rakotondrasoa, Eddie Fanantenana, Ranglack, Dustin H, Rankou, Hassan, Reardon, James Thomas, Richter, Stephen C, Rivers, Malin C, da Rosa, Patrícia, Royer, Emily, Salmon, Lily, Salvador, Carlos Henrique, Samways, Michael J, Sasaki, Hiroshi, Schutz, Emmanuel, Scott, Heather Ann, Scott, Robert Michael, Serena, Fabrizio, Sharma, Surya P, Shuey, John A, Silva, Carlos Julio Polo, Spaet, Julia LY, Sultana, Shanjida, Talukdar, Bibhab Kumar, Trinh-Dinh, Hoang, Tuboi, Chongpi, Virens, Jo, van Weerd, Merlijn, Weigmann, Simon, Willcox, Daniel

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    Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing von Sifrim, Alejandro, Hitz, Marc-Phillip, Wilsdon, Anna, Breckpot, Jeroen, Turki, Saeed H Al, Thienpont, Bernard, McRae, Jeremy, Fitzgerald, Tomas W, Singh, Tarjinder, Swaminathan, Ganesh Jawahar, Prigmore, Elena, Rajan, Diana, Abdul-Khaliq, Hashim, Banka, Siddharth, Bauer, Ulrike MM, Bentham, Jamie, Berger, Felix, Bhattacharya, Shoumo, Bu'Lock, Frances, Canham, Natalie, Colgiu, Irina-Gabriela, Cosgrove, Catherine, Cox, Helen, Daehnert, Ingo, Daly, Allan, Danesh, John, Fryer, Alan, Gewillig, Marc, Hobson, Emma, Hoff, Kirstin, Homfray, Tessa, INTERVAL Study, Kahlert, Anne-Karin, Ketley, Ami, Kramer, Hans-Heiner, Lachlan, Katherine, Lampe, Anne Katrin, Louw, Jacoba J, Manickara, Ashok Kumar, Manase, Dorin, McCarthy, Karen P, Metcalfe, Kay, Moore, Carmel, Newbury-Ecob, Ruth, Omer, Seham Osman, Ouwehand, Willem H, Park, Soo-Mi, Parker, Michael J, Pickardt, Thomas, Pollard, Martin O, Robert, Leema, Roberts, David J, Sambrook, Jennifer, Setchfield, Kerry, Stiller, Brigitte, Thornborough, Chris, Toka, Okan, Watkins, Hugh, Williams, Denise, Wright, Michael, Mital, Seema, Daubeney, Piers EF, Keavney, Bernard, Goodship, Judith, UK10K Consortium, Abu-Sulaiman, Riyadh Mahdi, Klaassen, Sabine, Wright, Caroline F, Firth, Helen V, Barrett, Jeffrey C, Devriendt, Koenraad, FitzPatrick, David R, Brook, J David, Deciphering Developmental Disorders Study, Hurles, Matthew E

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