检索结果 - Michèle Granier
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1
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects 由 Annie Laquerrière, Jérôme Maluenda, Adrien Camus, Laura Fontenas, Klaus Dieterich, Flora Nolent, Jie Zhou, Nicole Monnier, Philippe Latour, D. Gentil, D. Héron, I. Desguerres, P. Landrieu, Claire Bénéteau, B. Delaporte, Céline Bellesme, C. Baumann, Yline Capri, Alice Goldenberg, Stanislas Lyonnet, Dominique Bonneau, B. Estournet, Susana Quijano-Roy, Christine Francannet, S. Odent, Marie‐Hélène Saint‐Frison, Sabine Sigaudy, Dominique Figarella‐Branger, A. Gélot, J M Mussini, C. Lacroix, Valérie Drouin‐Garraud, Marie‐Claire Malinge, Tania Attié‐Bitach, B. Bessières, Maryse Bonnière, Férechté Encha‐Razavi, A. M. Beaufrére, S. Khung-Savatovsky, María José Pérez, Alexandre Vasiljevic, Sandra Mercier, J. Roume, Laetitia Trestard, Pascale Saugier‐Veber, Marie‐Pierre Cordier, Valérie Layet, Marine Legendre, Adeline Vigouroux‐Castera, Joël Lunardi, Mónica Bayés, Pierre‐Simon Jouk, Luc Rigonnot, Michèle Granier, Damien Sternberg, J. Warszawski, Marta Gut, M. Gonzalés, Marcel Tawk, Judith Melki
出版 2013Artigo -
2
Survival and Morbidity of Preterm Children Born at 22 Through 34 Weeks’ Gestation in France in 2011 由 Pierre‐Yves Ancel, François Goffinet, Pierre Kuhn, B. Langer, Jacqueline Matis, X. Hernandoréna, P. Chabanier, Laurence Joly-Pedespan, Bénédicte Lecomte, Françoise Vendittelli, Michel Dreyfus, B. Guillois, A. Burguet, P Sagot, Jacques Sizun, Alain Beuchée, Florence Rouget, Amélie Favreau, Élie Saliba, Nathalie Bednarek, P Morville, Gérard Thiriez, Loı̈c Marpeau, Stéphane Marret, Gilles Kayem, Xavier Durrmeyer, Michèle Granier, Olivier Baud, Pierre‐Henri Jarreau, Delphine Mitanchez, Pascal Boileau, Pierre Boulot, Gilles Cambonie, Hubert Daudé, A. Bédu, F. Mons, Jeanne Fresson, Rachel Vieux, Catherine Alberge, Catherine Arnaud, Christophe Vayssière, Patrick Truffert, Véronique Pierrat, D. Subtil, Claude D’Ercole, Catherine Gire, Umberto Siméoni, A. Bongain, Loı̈c Sentilhes, Jean‐Christophe Rozé, Jean Gondry, André Leke, Michel Deiber, Olivier Claris, Jean‐Charles Picaud, Anne Ego, Thierry Debillon, Anne Poulichet, Eliane Coliné, A. Favre, Olivier Fléchelles, Sylvain Sampériz, Duksha Ramful, B. Branger, Valérie Benhammou, L. Foix‐L’Hélias, Laetitia Marchand‐Martin, Monique Kaminski
出版 2015Artigo -
3
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita 由 Annie Laquerrière, Dana Jaber, Emanuela Abiusi, Jérôme Maluenda, Dan Mejlachowicz, Alexandre Vivanti, Klaus Dieterich, Radka Stoeva, Loïc Quevarec, Flora Nolent, Valérie Biancalana, Philippe Latour, Damien Sternberg, Yline Capri, Alain Verloès, Bettina Bessières, Laurence Lœuillet, Tania Attié‐Bitach, Jéléna Martinovic, Sophie Blesson, Florence Petit, Claire Bénéteau, Sandra Whalen, Florent Marguet, Jérôme Bouligand, Delphine Héron, Géraldine Viot, Jeanne Amiel, Daniel Amram, Céline Bellesme, Martine Bucourt, Laurence Faivre, Pierre‐Simon Jouk, Suonavy Khung, Sabine Sigaudy, Anne‐Lise Delezoide, Alice Goldenberg, Marie‐Line Jacquemont, Laëtitia Lambert, Valérie Layet, Stanislas Lyonnet, Arnold Münnich, Lionel Van Maldergem, Juliette Piard, Fabien Guimiot, P. Landrieu, Pascaline Létard, Fanny Pelluard, Laurence Perrin, Marie‐Hélène Saint‐Frison, Haluk Topaloğlu, Laetitia Trestard, Catherine Vincent‐Delorme, Helge Amthor, Christine Barnérias, Alexandra Benachi, Éric Bieth, Elise Boucher, Valérie Cormier‐Daire, Andrée Delahaye‐Duriez, Isabelle Desguerre, B. Eymard, Christine Francannet, Sarah Grotto, Didier Lacombe, Fanny Laffargue, Marine Legendre, Dominique Martin–Coignard, André Mégarbané, Sandra Mercier, Mathilde Nizon, Luc Rigonnot, Fabienne Prieur, Chloé Quēlin, Hanitra Ranjatoelina-Randrianaivo, Nicoletta Resta, Annick Toutain, Hélène Verhelst, Marie Vincent, Estelle Colin, Catherine Fallet‐Bianco, Michèle Granier, R Grigorescu, Julien Saada, Marie Gonzalès, Anne Guiochon‐Mantel, Jean‐Louis Bessereau, Marcel Tawk, Marta Gut, Cyril Gitiaux, Judith Melki
出版 2021Artigo
相关主题
Biology
Genetics
Arthrogryposis
Arthrogryposis multiplex congenita
Exome sequencing
Gene
Axolemma
Bioinformatics
Bronchopulmonary dysplasia
Candidate gene
Cell biology
Central nervous system
Cohort
Cohort study
DNA sequencing
Disease gene identification
Environmental health
Exome
Frameshift mutation
Genetic heterogeneity
Gestation
Gestational age
Internal medicine
Intraventricular hemorrhage
Medicine
Mutation
Myelin
Necrotizing enterocolitis
Neuroscience
Obstetrics