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Showing articles 0 to 7 of 7 Filter Applied: short stature (Click to remove) Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification NEJM 313:139-181, Sly,W.S.,et al, 1985 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 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 Paraparesis in Hereditary Multiple Exostoses:Case Report Neurol 29:973-977, Ferrari,G.,et al, 1979 Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue (Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972 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 7 of 7