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European Journal of Human Genetics : EJHG|January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in EuropeS Akli, J Boue, K Sandhoff, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 20, 1994
Enzyme replacement in a canine model of Hurler syndromeR M Shull, E D Kakkis, M F McEntee, et al.
Journal of Inherited Metabolic Disease|September 19, 2007
Effect of 'attenuated' mutations in mucopolysaccharidosis IVA on molecular phenotypes of N-acetylgalactosamine-6-sulfate sulfataseA M Montaño, K Sukegawa, Z Kato, et al.
Journal of Medical Genetics|June 1, 1991
Sanfilippo syndrome type D in two adolescent sistersL Siciliano, A Fiumara, L Pavone, et al.
Pediatrics|January 1, 1976
The iduronidase-deficient mucopolysaccharidoses: clinical and roentgenorgraphic featuresR E Stevenson, R R Howell, V A McKusick, et al.
American Journal of Human Genetics|April 1, 1986
Two abnormalities of hexosaminidase A in clinically normal individualsE E Grebner, D A Mansfield, S S Raghavan, et al.
Gene Therapy|May 1, 1997
In vitro correction of iduronate-2-sulfatase deficiency by adenovirus-mediated gene transferC Di Francesco, C Cracco, R Tomanin, et al.
The Journal of Biological Chemistry|April 5, 1992
Cloning and characterization of cDNA encoding canine alpha-L-iduronidase. mRNA deficiency in mucopolysaccharidosis I dogL J Stoltzfus, B Sosa-Pineda, S M Moskowitz, et al.
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