gène (2) Patients (2) Patients (2) mise sous écran protecteur (1) région (1) mutation (1) gestion (1) famille (1) effet (1) maladie (1) enfant (1) index (1) Defects (1) Implements (1) Methods (1) Identification (1) Abnormalities (1) Phenotype (1) Tools (1) Tissues (1) Stature, Short (1) Relevance (1) Mosaicism (1) Methylation (1) Messenger RNA (1) Management (1) Kabuki (1) Islands (1) Identification (1) Fragile X syndrome (1)