1. Fabry's disease: normal a-galactosidase activity and urinarysediment glycosphingolipid levels in two obligate heterozygotes;Avila, J.L.; Convit, J.; Avila, G.V.;British Journal of Dermatology,1973
2. Biochemical and electrophoretic studies of a-galactosidase in normal man, in patients with Fabry's disease, and in Equidae;Beutler, E.; Kuhl, W.;American Journal of Human Genetics,1972
3. Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency;Brady, R.O.; Gal, A.E.; Bradley, R.M.; Martensson, E.; Warshaw, A.L.; Laster, L.;New England Journal of Medicine,1967
4. Hurler's syndrome: a genetic study of clones in cell culture with particular reference to the Lyon hypothesis;Danes, B.S.; Bearn, A.G.;Journal of Experimental Medicine,1967
5. Demonstration of two populations of cells in the human female heterozygous for glucose-6-phosphate dehydrogenase variants;Davidson, R.G.; Notowsky, H.M.; Childs, B.;Proceedings of the National Academy of Sciences of the United States ofAmerica,1963