Treffer 1 - 20 von 24 für Suche 'Skinner, Claire F', Suchdauer: 1,72s Treffer weiter einschränken
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    CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language von Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

    Veröffentlicht in Nature communications

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    Mesh inlay, mesh kit or native tissue repair for women having repeat anterior or posterior prolapse surgery: randomised controlled trial (PROSPECT) von Hemming, C, Freeman, RM, Smith, ARB, Hagen, S, Montgomery, I, Kilonzo, M, Boyers, D, McDonald, A, McPherson, G, Reid, FM, Terry, Peter, Fattah, Mohamed Abdel, Swan, Lynn, Dallas, Christine, Allan, Angela, Henderson, Christina, Agur, Wael, Henry, Margo, Gilmour, Danielle, Farag, Khalid, Dass, Meenakshi, Reid, Michelle, Toozs‐Hobson, Philip, Latthe, Pallavi, Parsons, Matthew, Williams, Abimbola, Chia, Philip, Rhead, Katrina, Mistry, Raksha, Calvert, Sue, Bowyer, Anne, Cloete, Jenny, Archer, Denise, Kearsley, Nichola, Devlin, Hollie, Matar, Mohamed, Wilson, Toni, Bennett, Caroline, Chan, Yi Ling, Bondili, A, Kitchingman, Judith, Bexhell, Helen, Digesu, Alex, Underwood, Jenny, Singh, Anand, Tincello, Douglas, Fowler, Victoria, Christie, Carla, Fayyad, Abdalla, Bastion, Victoria, Smith, Anthony, Rose, Karen, Green, Linda, Biancardi, Rachel, Kumakech, Wilfred, Connell, Rowan, Lord, Susan, Jones, Sharon, Nolan, Tracey, Casey, Rebecca, Fishwick, Kathryn, Lowry, Tracey, Buckley, Sarah, Townend, Claire, Eckford, Seumas, Eskander, Osama, Belcher, Geraldine, Skinner, Amanda, Passmore, Deborah, Hooper, Paul, Das, Mausumi, Hickman, Emma, Heawood, Sarah, Bombieri, Luigi, Brockman, Paula, King, Angela, Hogston, Patrick, Parkinson, Richard, Jenkins, Elinor, Prashar, Sanjeev, Butler, Julie, Patel, Daksha, Field, Janet, Walker, Rachel, Cunningham, Mishell, Pearson, Sally Anne, Sturley, Rachel, Renton, Caroline, Ballard, Paul, Anderson, Colette, Potts, Julie, Chamberlain, Jonathan, Mercer, Pauline, Visvanathan, Shankar, Dawlatly, Bashir, Maseko, Zandile, El Naqa, Ayman, Afifi, Khaled, Kempson, Sharon, Denyer, Nick


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    Symptom-based stratification of patients with primary Sjögren's syndrome: multi-dimensional characterisation of international observational cohorts and reanalyses of randomised cli... von Tarn, Jessica R, Seror, Raphaele, McMeekin, Peter, Al-Ali, Shereen, Hackett, Katie L, Hargreaves, Ben, Price, Elizabeth, Pease, Colin T, Hunter, John, Gupta, Monica, Sutcliffe, Nurhan, Regan, Marian, Giles, Ian, Isenberg, David, McHugh, Neil, Young-Min, Steven, Akil, Mohammed, Stocken, Deborah, Everett, Colin, Gottenberg, Jacques-Eric, Devauchelle-Pensec, Valerie, Dieude, Philippe, Dubost, Jean Jacques, Fauchais, Anne-Laure, Goeb, Vincent, Larroche, Claire, Le Guern, Véronique, Morel, Jacques, Puéchal, Xavier, Tubiana, Sarah, Inamo, Karine, Molinari, Domitille, Baron, Gabriel, Saraux, Alain, Devauchelle-Pensec, Valérie, Hayem, Gilles, Hatron, Pierre, Sene, Damien, Zarnitsky, Charles, Perrodeau, Elodie, Mariette, Xavier, Pitzalis, C, Emery, P, Gray, J, Hulme, C, Pease, C, Price, E, Woods, C, Bowman, S, Ng, Wan-Fai, Frankland, Helen, Moots, Robert, Bombardieri, Michele, Pitzalis, Constantino, Sutcliffe, Nurhan, Dasgin, Joanne, Pease, Colin, Pickles, David, Regan, Marian, Kin, Jon King, Holt, Amanda, Kadiki, Lucy, Kaur, Daljit, Khan, Abdul, Cosier, Tracey, Panthakalam, Gupta, Monica, Stirton, Lesley, Ortiz, Gill, Price, Elizabeth, Pelger, Suzannah, Gorman, Claire, Rose, Ginny, Cuckow, Sue, Batley, Michael, Einosas, Ruby, Macleod, Iain, Locke, James, Legg, Sarah, Mirza, Kamran, Jones, Adrian, Lanyon, Peter, Muir, Alice, Pugmire, Susan, Watkins, Marianne, Field, Anne, Kaye, Stephen, McHugh, Neil, Dowden, Andrea, Akil, Mohammed, Godia, Olivia, Palmer, Lynne, Dasgupta, Bhaskar, Long, Pamela, Vermaak, Erin, Chandra, Usha, MacKay, Kirsten, Fedele, Stefano, Ahwiren, Nyarko, Allcoa, Paul

    Veröffentlicht in The Lancet. Rheumatology

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    Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language von Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

    Veröffentlicht in Nature communications

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    Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language von Blok, Lot Snijders, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

    Veröffentlicht in Nature communications

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