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Showing articles 0 to 12 of 12 Filter Applied: genetic diagnosis,prenatal (Click to remove) Huntingtons Disease BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Aicardi-Gouti�res Syndrome Br Med Bull 89:183-201, Orcesi, S.,et al, 2009 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease Neurol 44:288-290, Meiner,V.,et al, 1994 Genetic Diagnosis of Gaucher's Disease Lancet 339:889-892, Mistry,P.K.,et al, 1992 The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture Neurol 38:1617-1627, Moser,H.W., 1988 The Cerebrohepatorenal (Zellweger) Syndrome NEJM 310:1141-1146, Moser,A.E.,et al, 1984 CT Scans in Menkes Disease Neurol 29:304-312, Seay,A.R.,et al, 1979 Prenatal Genetic Diagnosis NEJM 283:1370, Milunsky,A.,et al, 1970 Showing articles 0 to 12 of 12