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Showing articles 0 to 10 of 10 Filter Applied: prenatal diagnosis by amniocentesis (Click to remove) New Strategy for Prenatal Diagnosis of X-Linked Disorders NEJM 346:1502, Costa,J.,et al, 2002 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 Miller-Dieker Syndrome:Detection of a Cryptic Chromosome Translocation Using in Situ Hybridization in a Family Am J Dis Child 147:1291-1294, Alvarado,M.,et al, 1993 Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test JAMA 270:1569-1575, Brown,W.,et al, 1993 Outlook for the Child with a Cephalocele Pediatrics 90:914-919, Brown,M.S.,et al, 1992 Cesarean Section Before Onset of Labor & Motor Function in Infants with Meningomyelocele Diag Antenatally NEJM 324:662-666, 6901991., Luthy,D.S.,et al, 1991 Anderson-Fabray Disease, A Commonly Missed Diagnosis BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988 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 Congenital Toxoplasmosis Lancet 1:500-504, Desmonts,G.,et al, 1985 Showing articles 0 to 10 of 10