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American Journal of Human Genetics|July 1, 1979
Apparent hexosaminidase B deficiency in two healthy members of a pedigreeP Hechtman, A RowlandsBiochemical Genetics|October 1, 1988
Genetic control of ganglioside biosynthesis in miceD Sokoloff, P HechtmanJournal of Bacteriology|November 1, 1970
Neutral amino acid transport in Pseudomonas fluorescensP Hechtman, C R ScriverAmerican Journal of Human Genetics|November 1, 1990
More than one mutant allele causes infantile Tay-Sachs disease in French-CanadiansP Hechtman, F Kaplan, J Bayleran, et al.American Journal of Human Genetics|June 1, 1994
Four novel PEPD alleles causing prolidase deficiencyP Ledoux, C Scriver, P HechtmanClinica Chimica Acta; International Journal of Clinical Chemistry|November 15, 1984
Synthesis of 4-methylumbelliferyl-beta-D-N-acetylglucosamine-6-sulfate and its use in classification of GM2 gangliosidosis genotypesJ Bayleran, P Hechtman, W SarayClinical Genetics|September 1, 1983
A new form of residual hexosaminidase activity in infantile Tay Sachs disease fibroblastsP Hechtman, K Khoo, C IsaacsCanadian Journal of Biochemistry and Cell Biology = Revue Canadienne De Biochimie Et Biologie Cellulaire|August 1, 1985
Substrate binding properties of the human liver hexosaminidase A activator proteinP Hechtman, C Isaacs, L Smith-JonesAmerican Journal of Human Genetics|November 1, 1996
Expression and molecular analysis of mutations in prolidase deficiencyP Ledoux, C R Scriver, P HechtmanClinical Genetics|May 1, 1989
The mutation mechanism causing juvenile-onset Tay-Sachs disease among LebaneseP Hechtman, B Boulay, J Bayleran, et al.Pageof 26