De Baere,Elfride

Institution: Ghent University Hospital, Belgium

Research Interests: Syndrome, Gene, Mutations, Disease, Blepharophimosis, Genes, Patients, Genotype, Mutation, Phenotype, Retinal, Human, Eyelids, PCR, Recombination, Blindness, Eyelid, Genetic Testing, Genotype-phenotype Correlations, Premature Ovarian Failure