Enter your terms above and click the 'Search' button.

Showing articles 0 to 10 of 10 Filter Applied: prenatal diagnosis by amniocentesis (Click to remove) Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 Outlook for the Child with a Cephalocele Pediatrics 90:914-919, Brown,M.S.,et al, 1992 Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 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 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 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 Showing articles 0 to 10 of 10