spectacle (2) analyse (2) Deletion (2) Phenotype (2) Genes (2) Patients (2) Human beings (2) Eye (2) Abnormalities, Human (2) Analysis (2) Patients (2) nourisson (1) région (1) protéine (1) organe (1) mutation (1) mutant (1) marqueur (1) anticorps (1) trouble de l'audition (1) gène (1) ADN (1) Development (1) Methods (1) Identification (1) Abnormalities (1) Oligonucleotides (1) In situ hybridization (1) Will (1) RNA (1)