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Showing articles 0 to 8 of 8 Filter Applied: short stature (Click to remove) Craniofacial and Cutaneous Findings Expand the Phenotype of Hereditary Neuralgic Amyotrophy Neurol 57:1963-1968, Jeannet,P.,et al, 2001 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Cockayne Syndrome: Review of 140 Cases Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992 A Clinical Study of Noonan Syndrome Arch Dis Child 67:178-183, Sharland, M.,et al, 1992 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984 Clinicopathological Conference Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983 Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease (Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 1983 Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue (Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972 Showing articles 0 to 8 of 8