исследовательская статья
A Novel Mutation Involving the Initiation Codon of FGF3 in a Family Described with Complete Inner Ear Agenesis, Microtia and Major Microdontia (LAMM Syndrome)
Elise Schaefer, Maryline Minoux, Julia Lauer, Valérie Pelletier, Matthieu Schmittbuhl, Marie-Cécile Manière, François Clauss, Françis Veillon, Sophie Riehm, Corinne Stoetzel and Helene Dollfus