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Showing articles 0 to 8 of 8 Filter Applied: prenatal diagnosis by amniocentesis (Click to remove) 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 Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989 Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987 Effective Strategy for Prenatal Prediction of Duchenne & Becker Muscular Dystrophy Lancet 2:1294-1296, Forrest,S.M.,et al, 1987 Prenatal Diagnosis & Carrier Detection of Duchenne Muscular Dystrophy with Closely Linked RFLPs Lancet 1:655-658, Bakker,E.,et al, 1985 Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing J Pediatr 120:394-398, Hofman,K.J.&Boehm,C.D., 1992 Showing articles 0 to 8 of 8