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Showing articles 0 to 6 of 6 Filter Applied: DNA probes (Click to remove) Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations Neurol 47:1269-1277, Baser,M.E., 1996 A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996 Screening for von Hippel-Lindau Disease by DNA Polymorphism Analysis JAMA 267:1226-1231, Glenn,G.M.,et al, 1992 Genetic Testing for Huntington's Disease BMJ 300:1089-1090, Harper,P.,et al, 1990 Uptake of Presymptomatic Predictive Testing for Huntington's Disease Lancet 2:603-605, Craufurd,D.,et al, 1989 Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening Lancet 2:425-427, Greenberg,C.R.,et al, 1988 Showing articles 0 to 6 of 6