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Showing articles 0 to 7 of 7 Filter Applied: genetic diagnosis,prenatal (Click to remove) Adrenoleukodystrophy JAMA 294:3131-3134, Moser,H.W.,et al, 2005 Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test JAMA 270:1569-1575, Brown,W.,et al, 1993 Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era JAMA 270:2307-2315, Kaback,M.,et al, 1993 Detection of Full Fragile X Mutation Lancet 339:271-272, Pergolizzi,R.G.,et al, 1992 Population Screening for Fragile X Lancet 339:1210-1213, Turner,G.,et al, 1992 Uptake of Presymptomatic Predictive Testing for Huntington's Disease Lancet 2:603-605, Craufurd,D.,et al, 1989 Preventive Screening for Fragile X Syndrome Editorial, Lancet 2:1191-11921986., , 1986 Showing articles 0 to 7 of 7