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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 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy JNNP 63:4-14, vanGeel,B.M.,et al, 1997 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 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 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 The Cerebrohepatorenal (Zellweger) Syndrome NEJM 310:1141-1146, Moser,A.E.,et al, 1984 Showing articles 0 to 8 of 8