1. Chondroitinsulphaturia with a-L-iduronidase deficiency;Babarik, A.; Benson, P.F.; Dean, M.F.; Muir, H.;Lancet,1974
2. deficiency (mucopolysaccharidosis Type VII);Beaudet, A.L.; Di Ferrante, N.M.; Ferry, G.D.; Nichlas, Jr, B.L.;Birth Defects: Original Article Series,1974
3. A form of mucopolysaccharidosis with visceral storage and excessive urinary excretion of chondroitin sulphate;Benson, P.F.; Dean, M.F.; Muir, H.;Developmental Medicine and Child Neurology,1972
4. Different clinical and biochemical phenotypes associated with,-glucuronidase deficiency;Danes, B.S.; Degnan, M.;Birth Defects: Original Article Series,1974
5. The Hurler syndrome: a study of cultured lymphoid cell lines;Danes, B.S.; Hiutteroth, T.H.; Cleve, H.; Bearn, A.G.;Journal of Experimental Medicine,1972