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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.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.Genomics|May 15, 1994
Homology between a human protein and a protein of the green garden peaP Lee, W Kuhl, T Gelbart, et al.Proceedings of the Association of American Physicians|May 1, 1996
Gaucher disease: four families with previously undescribed mutationsE Beutler, T Gelbart, D Balicki, et al.Genomics|January 1, 1989
The human glucocerebrosidase gene and pseudogene: structure and evolutionM Horowitz, S Wilder, Z Horowitz, et al.Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989
Evolution of the genome and the genetic code: selection at the dinucleotide level by methylation and polyribonucleotide cleavageE Beutler, T Gelbart, J H Han, et al.Pageof 58