Lacombe,Denis

Institution: Catholic University Leuven, Belgium

Research Interests: Gene, Mutations, Phenotype, Syndrome, Atrophy, Carrying, Connexin 43, Cx43, Enamel, Enamel Hypoplasia, Families, Fingers, Genotype, Genotype-phenotype Correlation, Hypospadias, Mental Retardation, Microphthalmia, Mutation, Observation, Optic Atrophy