Filter Filter By date Start date End date By Team 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 Anne DUMAINE 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 0 results match your search. Publications A RAB27A duplication in several cases of Griscelli syndrome type 2: An... Publications Update of Thyroid Developmental Genes. Publications Fibrillarin is essential for S-phase progression and neuronal differentiation... Publications Genotype-phenotype correlations in individuals with pathogenic RERE va... Publications A neuropathological study of novel RTTN gene mutations causing a familial... Publications Reply: The expanding neurological phenotype of DNM1L-related disorders... Publications FAM46A mutations are responsible for autosomal recessive osteogenesis ... Publications FAM46A mutations are responsible for autosomal recessive osteogenesis ... Publications Shared genetic predisposition in rheumatoid arthritis-interstitial lung... Publications Using Drosophila nephrocytes in genetic kidney disease. Publications A Clinician Friendly Data Warehouse Oriented Toward Narrative Reports:... Publications Disease Evolution and Response to Rapamycin in Activated Phosphoinositide... Publications Gene-corrected human Munc13-4-deficient CD8+ T cells can efficiently restrict... Publications No correlation between mtDNA amount and methylation levels at the CpG island... Publications Mutations in TUBB4B Cause a Distinctive Sensorineural Disease. Pagination First page Previous Page … Page 31 Page 32 Page 33 Page 34 Current page 35 Page 36 Page 37 Page 38 Page 39 … Page Next Last page Newsletter Discoveries, advances, portaits... Find out the latest research news and medical innovations. Votre email Valider Data Privacy Policy
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