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Blood|April 1, 1992
Mutations in Jewish patients with Gaucher diseaseE Beutler, T Gelbart, W Kuhl, et al.Blood|January 1, 1990
Gamma-glutamylcysteine synthetase deficiency and hemolytic anemiaE Beutler, R Moroose, L Kramer, et al.DNA (Mary Ann Liebert, Inc.)|March 1, 1988
Structural analysis of the human glucocerebrosidase genesO Reiner, M Wigderson, M HorowitzJournal of Molecular Neuroscience : MN|January 1, 1989
Human sphingolipid activator protein-1 and sphingolipid activator protein-2 are encoded by the same geneO Reiner, O Dagan, M HorowitzBlood Cells, Molecules & Diseases|January 1, 1995
Five new Gaucher disease mutationsE Beutler, T Gelbart, A Demina, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1985
Heterogeneity in type I Gaucher disease demonstrated by restriction mapping of the geneJ Sorge, T Gelbart, C West, et al.Proceedings of the National Academy of Sciences of the United States of America|December 1, 1991
Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous stateE Beutler, T Gelbart, W Kuhl, et al.American Journal of Human Genetics|October 1, 1991
High frequency of the Gaucher disease mutation at nucleotide 1226 among Ashkenazi JewsA Zimran, T Gelbart, B Westwood, et al.Blood Cells, Molecules & Diseases|June 27, 1998
The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphismsP L Lee, T Gelbart, C West, et al.Gene|December 15, 1990
Prevalent and rare mutations among Gaucher patientsN Eyal, S Wilder, M HorowitzPageof 234