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The Journal of Pediatrics|February 1, 1984
Congenital ascites as a presenting sign of lysosomal storage diseaseJ E Gillan, J A Lowden, K Gaskin, et al.American Journal of Human Genetics|May 1, 1981
Heterozygote advantage in Tay-Sachs carriers?B Spyropoulos, P B Moens, J Davidson, et al.Journal of Molecular Biology|September 20, 1992
Crystallization of human beta-hexosaminidase BW B Church, L Swenson, M N James, et al.Clinical Biochemistry|April 1, 1985
HPLC analysis of urinary sulfatide: an aid in the diagnosis of metachromatic leukodystrophyP M Strasberg, I Warren, M A Skomorowski, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|July 31, 1983
HPLC analysis of neutral glycolipids: an aid in the diagnosis of lysosomal storage diseaseP M Strasberg, I Warren, M A Skomorowski, et al.Biochemical and Biophysical Research Communications|June 28, 1991
Isolation and expression of a full-length cDNA encoding the human GM2 activator proteinB Xie, B McInnes, K Neote, et al.FEBS Letters|September 12, 1988
Cloning and sequence analysis of a cDNA encoding the beta-subunit of mouse beta-hexosaminidaseB Bapat, M Ethier, K Neote, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1982
Evidence for two dissimilar polypeptide chains in the beta 2 subunit of hexosaminidaseD J Mahuran, F Tsui, R A Gravel, et al.Canadian Medical Association Journal|August 3, 1974
Screening for carriers of Tay-Sachs disease: A community projectJ A Lowden, S Zuker, A J Wilensky, et al.Journal of Lipid Research|July 1, 1979
Preparation of radiolabeled GM2 and GA2 gangliosidesA Novak, J A Lowden, Y L Gravel, et al.Pageof 8