nourisson (1) test (1) mutation (1) anion (1) gène (1) famille (1) ADN (1) vecteur (1) Causes (1) Diastrophic dwarfism (1) Methods (1) Phenotype (1) Site-specific mutagenesis (1) Dysplasia (1) Origin (1) Transportation (1) Transfection (1) Population (1) Patients (1) Parents (1) Ovaries (1) Human beings (1) Hypothesis (1) Hamsters (1) Families (1) Expression (1) DNA (1) Continuity (1) Chinese (1) Cells (1)