Hennekam,Raoul C M

Institution: Department of Clinical Genetics, Netherlands

Top Collaborators: Lombardi MP, Maas SM, Bellini C, Merks JH, Mannens MM, Smigiel R, Peeters B, Benninga MA, Biesecker LG, Kempers MJ, Van Der Horst CM, Vikkula M, Celli J, Hoek HW, Caron HN, Ozgen HM, Van Steensel MA, Schulte-merker S, Lampe A, Waterham HR

Research Interests: Mutations, Syndrome, Patients, Genes, Phenotype, Gene, Syndromes, Goltz-gorlin Syndrome, Gorlin Syndrome, Report, Human, Lymph, Regulation, Future, Focal Dermal Hypoplasia, Role, Silver, Diagnosis, Evaluation, Hydrops