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British Journal of Haematology|May 1, 1988
The in vivo ageing of red cell enzymes: direct evidence of biphasic decay from polycythaemic rabbits with reticulocytosisA Zimran, S Torem, E BeutlerMolecular Medicine (Cambridge, Mass.)|June 1, 1997
HLA-H and associated proteins in patients with hemochromatosisE Beutler, C West, T GelbartActa Haematologica|January 1, 1991
Definition of the mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD 'LeJeune'E Beutler, B Westwood, W KuhlAmerican Journal of Human Genetics|September 1, 1975
Hexosaminidase isozyme in type O Gm2 gangliosidosis (Sandhoff-Jatzkewitz disease)E Beutler, W Kuhl, D ComingsHuman Genetics|June 1, 1994
Tight linkage of pyruvate kinase (PKLR) and glucocerebrosidase (GBA) genesD Glenn, T Gelbart, E BeutlerJournal of Clinical Psychology|April 17, 1998
Clinical utility research: an introductionL E Beutler, K I HowardHematopathology and Molecular Hematology|June 3, 1998
Structure and linkage relationships of the region containing the human L-type pyruvate kinase (PKLR) and glucocerebrosidase (GBA) genesA Demina, E Boas, 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 GelbartJournal of Clinical Psychology|September 12, 2003
Coping and coping styles in personality and treatment planning: introduction to the special seriesLarry E Beutler, Rudolf H MoosGenomics|April 1, 1992
Polymorphisms in the human glucocerebrosidase geneE Beutler, C West, T GelbartPageof 667