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Blood Cells, Molecules & Diseases|August 22, 2000
A common intron 3 mutation (IVS3 -48c-->g) leads to misdiagnosis of the c.845G-->A (C282Y) HFE gene mutationE Beutler, T GelbartHuman Mutation|January 1, 1994
Erroneous assignment of Gaucher disease genotype as a consequence of a complete gene deletionE Beutler, T GelbartThe Journal of Laboratory and Clinical Medicine|May 1, 1985
Plasma glutathione in health and in patients with malignant diseaseE Beutler, T GelbartGenetic Testing|August 23, 2000
Large-scale screening for HFE mutations: methodology and costE Beutler, T GelbartBritish Journal of Haematology|October 1, 1993
Gaucher disease mutations in non-Jewish patientsE Beutler, T GelbartClinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1986
Improved assay of the enzymes of glutathione synthesis: gamma-glutamylcysteine synthetase and glutathione synthetaseE Beutler, T GelbartBlood|May 29, 2000
Estimating the prevalence of pyruvate kinase deficiency from the gene frequency in the general white populationE Beutler, T GelbartAmerican Journal of Clinical Pathology|December 1, 1981
Falsely normal value in fluorometric transferase screening of galactosemic blood. A cautionary noteE Beutler, T GelbartBlood Cells, Molecules & Diseases|January 1, 1997
HLA-H mutations in the Ashkenazi Jewish populationE Beutler, T GelbartPageof 42