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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 Rowlands
Biochemical Genetics|October 1, 1988
Genetic control of ganglioside biosynthesis in miceD Sokoloff, P Hechtman
DNA and Cell Biology|October 1, 1993
Tay-Sachs disease screening and diagnosis: evolving technologiesP Hechtman, F Kaplan
Annales De Chirurgie De La Main Et Du Membre Superieur : Organe Officiel Des Societes De Chirurgie De La Main = Annals of Hand and Upper Limb Surgery|January 1, 1997
[Failure of total uncemented trapeziometacarpal prosthesis. A multicenter study]P Ledoux
Journal of Bacteriology|November 1, 1970
Neutral amino acid transport in Pseudomonas fluorescensP Hechtman, C R Scriver
Science (New York, N.Y.)|August 27, 1971
Serum parathyroid hormone in X-linked hypophosphatemiaC Arnaud, F Glorieux, C Scriver
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
The GM2 gangliosidoses databases: allelic variation at the HEXA, HEXB, and GM2A gene lociP Cordeiro, P Hechtman, F Kaplan
Clinica 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 Saray
Clinical Genetics|September 1, 1983
A new form of residual hexosaminidase activity in infantile Tay Sachs disease fibroblastsP Hechtman, K Khoo, C Isaacs
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