Phenotype (3) Mice (3) spectacle (2) risque (2) protéine (2) gène (2) Synapses (2) Risk (2) Patients (2) Human beings (2) Fragile X syndrome (2) Expression (2) Autism (2) Patients (2) puits (1) comportement (1) association (1) architecture (1) modèle (1) perte (1) information (1) famille (1) enfant (1) abords (agglomération) (1) Defects (1) Area (1) Observations (1) Observations (1) Drama (1) Abnormalities (1)