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Human Molecular Genetics|November 1, 1993
Cloning and expression of cDNA encoding human galactocerebrosidase, the enzyme deficient in globoid cell leukodystrophyY Q Chen, M A Rafi, G de Gala, et al.Somatic Cell and Molecular Genetics|January 1, 1993
Mutational analysis in a patient with a variant form of Gaucher disease caused by SAP-2 deficiencyM A Rafi, G de Gala, X L Zhang, et al.Journal of Inherited Metabolic Disease|January 1, 1991
Complementation studies in human and caprine beta-mannosidosisP Hu, D A Wenger, O P van Diggelen, et al.The Journal of Laboratory and Clinical Medicine|November 1, 1981
Metabolism of fatty acid-labeled cerebroside sulfate in cultured cells from controls and metachromatic leukodystrophy patients. Use in the prenatal identification of a false positive fetusT Kudoh, M Sattler, J Malmstrom, et al.Cytogenetics and Cell Genetics|January 1, 1994
Regional mapping of the human galactocerebrosidase gene (GALC) to 14q31 by in situ hybridizationL A Cannizzaro, Y Q Chen, M A Rafi, et al.The Southeast Asian Journal of Tropical Medicine and Public Health|December 1, 1979
Niemann-Pick disease in association with homozygous hemoglobin E: a case reportV S Tanphaichitr, V Suvatte, S Tuchinda, et al.Human Mutation|January 1, 1994
Molecular genetics of metachromatic leukodystrophyV Gieselmann, J Zlotogora, A Harris, et al.Proceedings. Biological Sciences|September 4, 2003
Facultative sperm storage in response to nutritional status in a female insectS Roth, K ReinhardtPageof 116