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Showing articles 0 to 8 of 8 Filter Applied: genetic diagnosis,prenatal (Click to remove) Adrenoleukodystrophy JAMA 294:3131-3134, Moser,H.W.,et al, 2005 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Analysis of Dystrophin Expression after Activation of Myogenesis in Amniocytes, Chorionic-Villus Cells, and Fibroblasts NEJM 329:915-920, Sancho,S.,et al, 1993 Predictive Testing for Wilson's Disease Using Tightly Linked and Flanking DNA Markers Neurol 41:992-999, Farrer,L.A.,et al, 1991 Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14 Lancet 336:271-273, Melki,J.,et al, 1990 Predictive Testing for Huntington's Disease with Linked DNA Markers Lancet 2:463-466, Brock,D.J.H.,et al, 1989 Uptake of Presymptomatic Predictive Testing for Huntington's Disease Lancet 2:603-605, Craufurd,D.,et al, 1989 Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker NEJM 318:535-542, Meissen,G.J.,et al, 1988 Showing articles 0 to 8 of 8