检索结果 - Blanc, Xavier

Retrieval of Publications Addressing Shared Decision Making: An Evaluation of Full-Text Searches on Medical Journal Websites 由 Blanc, Xavier, Collet, Tinh-Hai, Auer, Reto, Iriarte, Pablo, Krause, Jan, Légaré, France, Cornuz, Jacques, Clair, Carole

获取全文 获取全文 获取全文

Extensive cellular heterogeneity of X inactivation revealed by single-cell allele-specific expression in human fibroblasts 由 Garieri, Marco, Stamoulis, Georgios, Blanc, Xavier, Falconnet, Emilie, Ribaux, Pascale, Borel, Christelle, Santoni, Federico, Antonarakis, Stylianos E.

获取全文 获取全文 获取全文

Publication trends of shared decision making in 15 high impact medical journals: a full-text review with bibliometric analysis 由 Blanc, Xavier, Collet, Tinh-Hai, Auer, Reto, Fischer, Roland, Locatelli, Isabella, Iriarte, Pablo, Krause, Jan, Légaré, France, Cornuz, Jacques

获取全文 获取全文 获取全文

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations 由 Rodan, Lance H., Spillmann, Rebecca C., Kurata, Harley T., Lamothe, Shawn M., Maghera, Jasmine, Jamra, Rami Abou, Alkelai, Anna, Antonarakis, Stylianos E., Atallah, Isis, Bar-Yosef, Omer, Bilan, Frédéric, Bjorgo, Kathrine, Blanc, Xavier, Van Bogaert, Patrick, Bolkier, Yoav, Burrage, Lindsay C., Christ, Björn U., Granadillo, Jorge L., Dickson, Patricia, Donald, Kirsten A., Dubourg, Christèle, Eliyahu, Aviva, Emrick, Lisa, Engleman, Kendra, Gonfiantini, Michaela Veronika, Good, Jean-Marc, Kalser, Judith, Kloeckner, Chiara, Lachmeijer, Guus, Macchiaiolo, Marina, Nicita, Francesco, Odent, Sylvie, O’Heir, Emily, Ortiz-Gonzalez, Xilma, Pacio-Miguez, Marta, Palomares-Bralo, María, Pena, Loren, Platzer, Konrad, Quinodoz, Mathieu, Ranza, Emmanuelle, Rosenfeld, Jill A., Roulet-Perez, Eliane, Santani, Avni, Santos-Simarro, Fernando, Pode-Shakked, Ben, Skraban, Cara, Slaugh, Rachel, Superti-Furga, Andrea, Thiffault, Isabelle, van Jaabrsveld, Richard H., Vincent, Marie, Wang, Hong-Gang, Zacher, Pia, Rush, Eric, Pitt, Geoffrey, Au, Ping Yee Billie, Shashi, Vandana

获取全文 获取全文 获取全文

De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability 由 Schalk, Audrey, Cousin, Margot A., Dsouza, Nikita R., Challman, Thomas D., Wain, Karen E., Powis, Zöe, Minks, Kelly, Trimouille, Aurélien, Lasseaux, Eulalie, Lacombe, Didier, Angelini, Chloé, Michaud, Vincent, Van-Gils, Julien, Spataro, Nino, Ruiz, Anna, Gabau, Elizabeth, Stolerman, Elliot, Washington, Camerun, Louie, Raymond J., Lanpher, Brendan C, Kemppainen, Jennifer L., Innes, A. Micheil, Kooy, R. Frank, Meuwissen, Marije, Goldenberg, Alice, Lecoquierre, François, Vera, Gabriella, Diderich, Karin E M, Sheidley, Beth Rosen, Achkar, Christelle Moufawad El, Park, Meredith, Hamdan, Fadi F., Michaud, Jacques L., Lewis, Ann J., Zweier, Christiane, Reis, André, Wagner, Matias, Weigand, Heike, Journel, Hubert, Keren, Boris, Passemard, Sandrine, Mignot, Cyril, van Gassen, Koen L.I., Brilstra, Eva H., Itzikowitz, Gina, O’Heir, Emily, Allen, Jake, Donald, Kirsten A., Korf, Bruce R., Skelton, Tammi, Thompson, Michelle L, Robin, Nathaniel H., Rudy, Natasha, Dobyns, William B., Foss, Kimberly, Zarate, Yuri A, Bosanko, Katherine A., Alembik, Yves, Durand, Benjamin, Mau-Them, Frédéric Tran, Ranza, Emmanuelle, Blanc, Xavier, Antonarakis, Stylianos E., McWalter, Kirsty, Torti, Erin, Millan, Francisca, Dameron, Amy, Tokita, Mari J., Zimmermann, Michael T., Klee, Eric W., Piton, Amélie, Gerard, Bénédicte

获取全文 获取全文 获取全文