Zoekresultaten - Virginie Laugel-Haushalter
- Toon 1 - 3 resultaten van 3
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1
Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop’s classification door Agnès Bloch‐Zupan, Tristan Rey, Alexandra Jimenez-Armijo, Marzena Kawczynski, Naji Kharouf, Muriel De La Dure‐Molla, Emmanuelle Noirrit‐Esclassan, Magali Hernandez, Clara Joseph-Beaudin, Séréna Lopez-Cazaux, C Tardieu, Béatrice Thivichon‐Prince, Taťjana Dostálová, Milan Maçek, Mustapha El Alloussi, Leila Qebibo, Supawich Morkmued, Patimaporn Pungchanchaikul, Blanca Urzúa Orellana, Marie-Cécile Manière, Bénédicte Gérard, Isaac Maximiliano Bugueno, Virginie Laugel-Haushalter
Gepubliceerd in 2023Artigo -
2
Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta door Mathilde Huckert, Corinne Stoetzel, Supawich Morkmued, Virginie Laugel-Haushalter, Véronique Geoffroy, Jean Muller, François Clauss, Megana Prasad, Frédéric Obry, Jean Louis Raymond, Marzena Switala, Yves Alembik, S. Soskin, Éric Mathieu, Joseph Hemmerlé, Jean‐Luc Weickert, Branka Dabovic, Daniel B. Rifkin, Annelies Dheedene, Eveline Boudin, Oana Caluseriu, Marie‐Claude Cholette, Ross McLeod, Reynaldo Antequera, Marie-Paule Gellé, Jean-Louis Coeuriot, L. F. Jacquelin, Isabelle Bailleul‐Forestier, Marie‐Cécile Manière, Wim Van Hul, Débora Romeo Bertola, Pascal Dollé, Alain Verloès, Geert Mortier, Hélène Dollfus, Agnès Bloch‐Zupan
Gepubliceerd in 2015Artigo -
3
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement door Megana Prasad, Véronique Geoffroy, Serge Vicaire, Bernard Jost, Michaël Dumas, Stéphanie Le Gras, Marzena Switala, Barbara Gasse, Virginie Laugel-Haushalter, Marie Paschaki, Bruno Leheup, D Droz, Amelie Dalstein, Adeline Loing, Bruno Grollemund, Michèle Muller‐Bolla, Séréna Lopez-Cazaux, Maryline Minoux, Sophie Jung, Frédéric Obry, Vincent Vogt, Jean‐Luc Davideau, Tiphaine Davit‐Béal, Anne-Sophie Kaiser, Ute Moog, Béatrice Richard, Jean-Jacques Morrier, Jean‐Pierre Duprez, Sylvie Odent, Isabelle Bailleul‐Forestier, M. Rousset, Laure Merametdijan, Annick Toutain, Clara Joseph, Fabienne Giuliano, Jean-Christophe Dahlet, Aymeric Courval, Mustapha El Alloussi, Samir Laouina, S. Soskin, Nathalie Guffon, Anne Dieux, Bérénice Doray, Stephanie Feierabend, Emmanuelle Ginglinger, Benjamin Fournier, Muriel De La Dure‐Molla, Yves Alembik, C Tardieu, François Clauss, Ariane Berdal, Corinne Stoetzel, M.C. Manière, Hélène Dollfus, Agnès Bloch‐Zupan
Gepubliceerd in 2015Artigo
Zoekinstrumenten:
Gerelateerde Onderwerpen
Amelogenesis imperfecta
Biology
Dentistry
Enamel paint
Gene
Genetics
Medicine
Osteogenesis imperfecta
Phenotype
Amelogenesis
Dentinogenesis imperfecta
Genetic heterogeneity
Pathology
Ameloblast
Anatomy
Bioinformatics
Cohort
Dental enamel
Disease
Etiology
Exome sequencing
Missense mutation
Mutation
Nonsense mutation
Pediatrics