1. Chondroitinsulphaturia with o-L-iduronidase deficiency;Babarik, A.; Benson, P.F.; Dean, M.F.; Muir, H.;Lancet,1974
2. Genetic errors of mucopolysaccharide degradation;Bach, G.; Cantz, M.; Hall, C.W.; Neufeld, E.F.;Biochemical Society Transactions,1973
3. The defect in the Hurler and Scheie syndromes: deficiency of a-L-iduronidase;Bach, G.; Friedman, R.; Weissmann, B.; Neufeld, E.F.;Proceedings of the National Academy of Sciences of the United States of America,1972
4. 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 Chlild Neurology,1972
5. In vitro confirmation ofgenetic compound of the Hurler and Scheie syndromes;Danes, B.S.;Lancet,1974