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Showing articles 0 to 9 of 9 Filter Applied: genetic diagnosis,prenatal (Click to remove) X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy JNNP 63:4-14, vanGeel,B.M.,et al, 1997 The Cerebrohepatorenal (Zellweger) Syndrome NEJM 310:1141-1146, Moser,A.E.,et al, 1984 Adrenoleukodystrophy JAMA 294:3131-3134, Moser,H.W.,et al, 2005 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 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 Myotonic Dystrophy In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994 The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture Neurol 38:1617-1627, Moser,H.W., 1988 Prenatal Diagnosis of Duchenne's Muscular Dystrophy NEJM 297:968, Mahoney,M.J.,et al, 1977 Showing articles 0 to 9 of 9