Hoefsloot,L H

Institution: Radboud University Nijmegen Medical Center, Netherlands

Top Collaborators: Schoots J, Hoenderop JG, Bergman JE, Glaudemans B, Yntema HG, San-cristobal P, Pfundt R, Kamsteeg EJ, Van Ravenswaaij-arts CM, Bindels RJ, Knoers NV, Ogata T, Sato N, Janssen N, Claahsen-van Der Grinten HL, Swertz MA, Van Der Donk K, Tranebjaerg L, Seminara S, Lodahl M

Research Interests: Mutations, Patients, Syndrome, Charge, Charge Syndrome, Gene, Phenotype, DNA, Regulation, Anosmia, Deafness, Ears, Genes, Hypogonadism, Hypogonadotropic Hypogonadism, Kallmann Syndrome, Semicircular Canals, Alkalosis, Exons, Family