Filter Filter Par date Date de début Date de fin Par équipe Michel Polak Alessandra Pierani Patrick Revy & Erika Brunet Sigolène Meilhac Laurent Abel Jeanne Amiel et Laurence Legeai‑Mallet Antonio Rausell Isabelle André Vincent Cantagrel Jean-Laurent Casanova Nadine Cerf-Bensussan Yanick Crow Olivier Hermine & Thiago Trovati Maciel Alain Hovnanian Edor Kabashi Sylvain Latour Valérie Cormier-Daire Mickaël Ménager Gaël Ménasché et Fernando Sepulveda Annarita Miccio Frédéric Rieux-Laucat Agnès Rötig Jean-Michel Rozet Sophie Saunier et Corinne Antignac Matias Simons Nathalie Boddaert Sabine Sarnacki et Isabelle Bloch Yves Ville Yakov VITRENKO Patrick Nitschké Corinne Cordier Meriem Garfa-Traoré Sylvie Fabrega Marie-Alexandra Alyanakian Sophie Berissi Chiara Guerrera Pierre David Nathalie Lefort Claude Besmond Marcelo Simon Sola LEAT Nathalie Boddaert Travail en collaboration : Unité de Recherche clinique-Centre d’investigation clinique (URC-CIC) Travail en collaboration : Département de Biothérapie, Centre d'Investigation Clinique pour les Thérapies Innovantes Salma Kotti Nicolas Garcelon Mickaël Ménager Michela Deleidi Annarita Miccio Annarita Miccio Jean Michel Rozet Sara Bizzotto Elodie Bal Bana Jabri Hossein Khonsari Karim Wahbi Lucile Couronné Denis Jabaudon, Thomas Blauwblomme et Rima Nabbout Bana Jabri Céline GRECO Filter Reset Résultat correspond à votre recherche Publications Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction... Publications Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct,... Publications Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leuko... Publications Biallelic mutations in neurofascin cause neurodevelopmental impairment... Publications De novo mutation screening in childhood-onset cerebellar atrophy identifies... Publications Whole-exome sequence analysis highlights the role of unmasked recessive... Publications High N-glycan multiplicity is critical for neuronal adhesion and sensitizes... Publications AMPA-receptor specific biogenesis complexes control synaptic transmission... Publications Effect of Cell-Free DNA Screening vs Direct Invasive Diagnosis on Miscarriage... Publications Utility of whole exome sequencing for the early diagnosis of pediatric-onset... Publications WDR81 mutations cause extreme microcephaly and impair mitotic progression... Publications Regulation of human cerebral cortical development by EXOC7 and EXOC8, components... Publications Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction... Publications 16p13.11p11.2 triplication syndrome: a new recognizable genomic disorder... Publications MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate... Newsletter Découvertes, avancées, portraits... retrouvez l'actualité de la recherche et les dernières innovations médicales. Votre email Valider Politique de confidentialité des données
