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Showing articles 0 to 13 of 13 Filter Applied: genetic diagnosis,prenatal (Click to remove) 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 Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 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 Myotonic Dystrophy In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994 Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism NEJM 327:57, Cossu,P.,et al, 1992 Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1) Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992 Predictive Testing for Wilson's Disease Using Tightly Linked and Flanking DNA Markers Neurol 41:992-999, Farrer,L.A.,et al, 1991 Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14 Lancet 336:271-273, Melki,J.,et al, 1990 The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture Neurol 38:1617-1627, Moser,H.W., 1988 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 Showing articles 0 to 13 of 13