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Showing articles 0 to 11 of 11 Filter Applied: prenatal diagnosis by amniocentesis (Click to remove) Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,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 Anderson-Fabray Disease, A Commonly Missed Diagnosis BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988 Effective Strategy for Prenatal Prediction of Duchenne & Becker Muscular Dystrophy Lancet 2:1294-1296, Forrest,S.M.,et al, 1987 Prenatal Diagnosis of Neuronal Ceroid Lipofuscinosis NEJM 310:595, MacLeod,P.M.,et al, 1984 Prenatal Genetic Diagnosis in 3000 Amniocenteses NEJM 300:157-163, Golbus,M.S.,et al, 1979 Infantile Metachromatic Leukodystrophy NEJM 288:1365, 14051973., Leroy,J.,et al, 1973 Showing articles 0 to 11 of 11