Search Results - Ash, Maria D.

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    Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome by Leiding, Jennifer W., Vogel, Tiphanie P., Smith, Madison R., Carisey, Alexandre, Vargas-Hernández, Alexander, Silva-Carmona, Manuel, Neven, Bénédicte, Ronan Leahy, Timothy, Taskinen, Mervi, Kostyuchenko, Larysa, Scherbina, Anna, Bauer, Cindy S., Giovannini-Chami, Lisa, Romberg, Neil, Prince, Benjamin T., Bohnsack, John, Pachlopnik Schmid, Jana, Bahna, Sami, Brothers, Shannon, Chan, Alice Y., Chandrakasan, Shanmuganathan, Christiansen, Mette, Cole, Theresa, Desai, Mukesh M., Gottrand, Frédéric, Grimbacher, Bodo, Hoffman, Hal M., Guerrerio, Anthony L., Kainulainen, Leena, Lawrence, Monica G., Martelius, Timi, Neth, Olaf, Lugo Reyes, Saúl Oswaldo, Russell, Mark A., Schejter, Yael, Skevofilax, Effie, Suan, Daniel, Velasco, Helena, Walkovich, Kelly, Aleshkevich, Svetlana, Allende, Luis M., Atschekzei, Faranaz, Aygunes, Utku, Barlogis, Vincent, Belko, John, Bezrodnik, Liliana, Biebl, Ariane, Caldirola, Maria Soledad, Castelle, Martin, Cokugras, Haluk, Cox, Fionnuala, Dalgic, Buket, ASH Dalm, Virgil, Dujovny, Tal, Eken, Ahmet, Fabre, Alexandre, Fischer, Alain, Hannibal, Mark, Huppert, Laura, Karakoc-Aydiner, Elif, Pac Kisaarslan, Ayşenur, Kiykim, Ayca, Klocperk, Adam, Kuzmenko, Natalia, Lianou, Dimitra, Lorenz, Myriam Ricarda, Manson, Ania, Marega, Lia Furlaneto, Nolan, David, Norlin, Anna-Carin, Oleastro, Matias, Ozcan, Alper, Picard, Capucine, Polychronopoulou, Sophia, Quesada, Juan Francisco, Randall, Katrina L., Resin, Geraldine, Rodina, Yulia, Rohrlich, Pierre, Sachs, Johnathan, Sakovich, Inga, Santarlas, Christopher, Scheffler Mendoza, Selma C., Schwarz, Klaus, Sediva, Anna, Slatter, Mary, Sleasman, John, Suratannon, Narissara, Tanita, Kay, Travis, Stephen, Tsinti, Maria, Unal, Ekrem, Urdinez, Luciano, Vazquez-Gomez, Felisa, Weiss, Mitchell J., Zhang, Yu, Seppänen, Mikko R.J., Sogkas, Georgios, Milner, Joshua D., Forbes Satter, Lisa R.

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    Widening of the genetic and clinical spectrum of Lamb–Shaffersyndrome, a neurodevelopmental disorder due to SOX5haploinsufficiency by Ash, Zawerton, Mignot Cyril, Sigafoos Ashley, Blackburn, Patrick R, Haseeb Abdul, McWalter Kirsty, Ichikawa Shoji, Nava, Caroline, Keren, Boris, Perrine, Charles, Marey Isabelle, Tabet Anne-Claude, Levy, Jonathan, Perrin, Laurence, Hartmann, Andreas, Lesca Gaetan, Schluth-Bolard Caroline, Monin, Pauline, Dupuis-Girod, Sophie, Guillen Sacoto Maria J, Schnur, Rhonda E, Zhu Zehua, Poisson, Alice, Salima, El Chehadeh, Alembik Yves, Ange-Line, Bruel, Lehalle Daphné, Nambot Sophie, Moutton Sébastien, Odent Sylvie, Jaillard Sylvie, Dubourg Christèle, Hilhorst-Hofstee Yvonne, Barbaro-Dieber Tina, Ortega, Lucia, Bhoj, Elizabeth J, Masser-Frye, Diane, Bird, Lynne M, Lindstrom, Kristin, Ramsey, Keri M, Narayanan Vinodh, Fassi, Emily, Willing, Marcia, Cole, Trevor, Salter, Claire G, Akilapa Rhoda, Vandersteen, Anthony, Canham, Natalie, Rump, Patrick, Gerkes, Erica H, Klein Wassink-Ruiter Jolien S, Bijlsma Emilia, Hoffer, Mariëtte J, Vargas, Marcelo, Wojcik Antonina, Cherik Florian, Francannet Christine, Rosenfeld, Jill A, Machol Keren, Scott, Daryl A, Bacino, Carlos A, Wang, Xia, Clark, Gary D, Bertoli, Marta, Zwolinski, Simon, Thomas, Rhys H, Akay Ela, Chang, Richard C, Bressi Rebekah, Sanchez Russo Rossana, Srour Myriam, Russell, Laura, Goyette, Anne-Marie E, Dupuis Lucie, Mendoza-Londono, Roberto, Karimov, Catherine, Maries, Joseph, Nizon Mathilde, Cogné Benjamin, Kuechler Alma, Piton Amélie, Klee, Eric W, Lefebvre Véronique, Clark, Karl J, Depienne Christel

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