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Showing articles 0 to 8 of 8 Filter Applied: prenatal diagnosis by amniocentesis (Click to remove) Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Miller-Dieker Syndrome:Detection of a Cryptic Chromosome Translocation Using in Situ Hybridization in a Family Am J Dis Child 147:1291-1294, Alvarado,M.,et al, 1993 Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing J Pediatr 120:394-398, Hofman,K.J.&Boehm,C.D., 1992 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 Effective Strategy for Prenatal Prediction of Duchenne & Becker Muscular Dystrophy Lancet 2:1294-1296, Forrest,S.M.,et al, 1987 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 Prenatal Diagnosis of Congenital Toxoplasmosis Lancet 1:500-504, Desmonts,G.,et al, 1985 Showing articles 0 to 8 of 8