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Showing articles 0 to 6 of 6 Filter Applied: DNA probes (Click to remove) Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 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 The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice Ann Neurol 32:207-214, Rowland,L.P., 1992 Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation NEJM 325:1673-1681, Rousseau,F.,et al, 1991 Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence NEJM 325:1720-1738, Sutherland,G.R.,et al, 1991 Molecular Genetics of Duchenne and Becker Muscular Dystrophy J Pediatr 117:1-15, Darras,B.T., 1990 Showing articles 0 to 6 of 6