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Blood Cells|January 1, 1986
The mechanism of removal of leukocytes by cellulose columnsE Beutler, T GelbartClinical and Laboratory Haematology|January 1, 1984
Globin-methionine complexes formed during labelling studiesE Beutler, T GelbartAnnals of Human Genetics|May 1, 1990
Gaucher disease associated with a unique KpnI restriction site: identification of the amino-acid substitutionE Beutler, T GelbartClinica Chimica Acta; International Journal of Clinical Chemistry|December 24, 1990
The facile detection of the nt 1226 mutation of glucocerebrosidase by 'mismatched' PCRE Beutler, T Gelbart, C WestMolecular Medicine (Cambridge, Mass.)|June 1, 1997
HLA-H and associated proteins in patients with hemochromatosisE Beutler, C West, T GelbartHuman Genetics|June 1, 1994
Tight linkage of pyruvate kinase (PKLR) and glucocerebrosidase (GBA) genesD Glenn, T Gelbart, E BeutlerProceedings of the National Academy of Sciences of the United States of America|June 1, 1985
6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiencyE Beutler, W Kuhl, T GelbartGenomics|April 1, 1992
Polymorphisms in the human glucocerebrosidase geneE Beutler, C West, T GelbartMolecular Medicine (Cambridge, Mass.)|November 1, 1994
Glucocerebrosidase mutations in Gaucher diseaseE Beutler, A Demina, T GelbartPageof 42