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Showing articles 0 to 8 of 8 Filter Applied: dysmorphic (Click to remove) Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 The Exercise Test in Andersen Syndrome Arch Neurol 56:352-356, Katz,J.S.,et al, 1999 Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 A Clinical Study of Noonan Syndrome Arch Dis Child 67:178-183, Sharland, M.,et al, 1992 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 Congenital Brain Anomalies Associated with the Hypoplastic Left Heart Syndrome Pediatrics 85:984-990, Glauser,T.A.,et al, 1990 Showing articles 0 to 8 of 8