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Showing articles 0 to 10 of 10 Filter Applied: genetic diagnosis,prenatal (Click to remove) Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 Huntingtons Disease BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010 Aicardi-Gouti�res Syndrome Br Med Bull 89:183-201, Orcesi, S.,et al, 2009 Adrenoleukodystrophy JAMA 294:3131-3134, Moser,H.W.,et al, 2005 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 Advances in Molecular Analysis of Fragile X Syndrome 552, Warren,W.T.&Nelson,D.L.JAMA 271:536-553, 1994 Myotonic Dystrophy In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994 CT Scans in Menkes Disease Neurol 29:304-312, Seay,A.R.,et al, 1979 Showing articles 0 to 10 of 10