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Showing articles 0 to 13 of 13 Filter Applied: genetic diagnosis,prenatal (Click to remove) Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 New Strategy for Prenatal Diagnosis of X-Linked Disorders NEJM 346:1502, Costa,J.,et al, 2002 The Muscular Dystrophies BMJ 317:991-995, Emery,A.E.H., 1998 X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy JNNP 63:4-14, vanGeel,B.M.,et al, 1997 Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995 Myotonic Dystrophy In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994 Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing J Pediatr 120:394-398, Hofman,K.J.&Boehm,C.D., 1992 Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 Prenatal Diagnosis of Cockayne's Syndrome Lancet 1:486-488, Lehmann,A.R.,et al, 1985 Prenatal Diagnosis of Fragile X Chromosome Lancet 1:99-100, Shapiro,L.R.,et al, 1982 Prenatal Genetic Diagnosis NEJM 283:1370, Milunsky,A.,et al, 1970 Showing articles 0 to 13 of 13