Frints,S G M

Institution: Department of Clinical Genetics, Netherlands

Top Collaborators: Weber JW, Stegmann AP, Vos YJ, Verhagen JM, Schrander-stumpel CT, De Die-smulders CE, Macville MV, Blezer MM, Schrander JJ, Rubio-gozalbo ME, Bakker JA, Van Winden LA, Van Lint FH, , Willekes C, Paulussen AD, Coumans AB, Gavilanes AW, Engelen JJ, Bakker J

Research Interests: Evaluation, Child, Congenital Hydrocephalus, Gene, Genetics, Hydrocephalus, Knowledge, L1cam, Patients, Survey, Syndrome, Chromosomal Abnormalities, Genes, Hemifacial Microsomia, Pathology, Syndrome, Walker-warburg, Walker, Walker-warburg Syndrome, Warburg Syndrome, Mutations