1. Occurrence of urinary acid mucopolysaccharides in the Hurler syndrome;Dorfman, A.; Lorincz, A.E.;Proc Natl Acad Sci USA,1957
2. Genetic heterogeneity and allelic variation in the mucopolysaccharidosis;McKusick, V.A.;Johns Hopkins Med J,1980
3. Beta glucuronidase deficiency: report of clinical, radiologic and biochemical features of a new mucopolysaccharidosis;Sly, W.S.; Quinton, B.A.; McAlister, W.H.; Rimoin, D.;J Pediatr,1973
4. A P-glucuronidase deficiency mucopolysaccharidosis: studies in cultured fibroblasts;Hall, C.W.; Cantz, M.; Neufeld, E.F.;Arch Biochem Biophys,1973
5. Different clinical and biochemical phenotypes associated with fl-glucuronidase deficiency;Danes, B.S.; Degnan, M.;Birth Defects,1974