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Showing articles 0 to 8 of 8 Filter Applied: prenatal diagnosis by amniocentesis (Click to remove) Anderson-Fabray Disease, A Commonly Missed Diagnosis BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988 Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 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 Outlook for the Child with a Cephalocele Pediatrics 90:914-919, Brown,M.S.,et al, 1992 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 Perinatal Neuropathy as an Early Manifestation of Krabbe's Disease Arch Neurol 37:446-447, Lieberman,J.S.,et al, 1980 Prenatal Genetic Diagnosis in 3000 Amniocenteses NEJM 300:157-163, Golbus,M.S.,et al, 1979 Showing articles 0 to 8 of 8