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Showing articles 0 to 10 of 10 Filter Applied: prenatal diagnosis by amniocentesis (Click to remove) Neurological Findings in Patients with the Fragile-X Syndrome JNNP 48:150-153, Finelli,P.F.,et al, 1985 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Practice Parameter,Management Issues for Women with Epilepsy (Summary Statement) Neurol 51:944-948, Rpt of the Quality Stnds Subcmte AAN, 1998 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 Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era JAMA 270:2307-2315, Kaback,M.,et al, 1993 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 Prenatal Prediction of Risk of the Fetal Hydantoin Syndrome NEJM 322:1567-1572, Buehler,B.A.,et al, 1990 Prenatal Genetic Diagnosis in 3000 Amniocenteses NEJM 300:157-163, Golbus,M.S.,et al, 1979 Showing articles 0 to 10 of 10