1. The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase;Bach, G.; Eisenberg, Jr., F.; Cantz, M.; Neufeld, E.F.;Proceedings ofthe National Academy of Sciences of the United States of America,1973
2. The defect in 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
3. In-vitro correction of deficient human fibroblasts by P-glucuronidase from different human sources;Brot, F.E.; Glaser, J.H.; Roozen, K.J.; Sly, W.S.; Stahl, P.D.;Biochemical and Biophysical Researcht Communications,1974
4. The Hunter corrective factor: purification and preliminary characterisation;Cantz, M.; Chrambach, A.; Bach, G.; Neufeld, E.F.;Journal of Biological Chemistry,1972
5. Dean, M. F., Benson, P. F., and Muir, H. (1973).