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Showing articles 0 to 12 of 12 Filter Applied: prenatal diagnosis by amniocentesis (Click to remove) New Strategy for Prenatal Diagnosis of X-Linked Disorders NEJM 346:1502, Costa,J.,et al, 2002 Analysis of Dystrophin Expression after Activation of Myogenesis in Amniocytes, Chorionic-Villus Cells, and Fibroblasts NEJM 329:915-920, Sancho,S.,et al, 1993 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 Prenatal Genetic Diagnosis in 3000 Amniocenteses NEJM 300:157-163, Golbus,M.S.,et al, 1979 Prenatal Diagnosis of Duchenne's Muscular Dystrophy NEJM 297:968, Mahoney,M.J.,et al, 1977 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 Anderson-Fabray Disease, A Commonly Missed Diagnosis BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988 The Cerebrohepatorenal (Zellweger) Syndrome NEJM 310:1141-1146, Moser,A.E.,et al, 1984 Showing articles 0 to 12 of 12