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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 Adrenoleukodystrophy JAMA 294:3131-3134, Moser,H.W.,et al, 2005 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 Predictive Testing for Huntington's Disease with Linked DNA Markers Lancet 2:463-466, Brock,D.J.H.,et al, 1989 Uptake of Presymptomatic Predictive Testing for Huntington's Disease Lancet 2:603-605, Craufurd,D.,et al, 1989 Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker NEJM 318:535-542, Meissen,G.J.,et al, 1988 The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture Neurol 38:1617-1627, Moser,H.W., 1988 CT Scans in Menkes Disease Neurol 29:304-312, Seay,A.R.,et al, 1979 Showing articles 0 to 10 of 10