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American 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 MoosJournal of Clinical Psychology|February 26, 2004
Virtual reality in psychotherapy trainingLarry E Beutler, T Mark HarwoodJournal of Clinical Psychology|March 16, 2006
Principles of therapeutic change: a task force on participants, relationships, and techniques factorsLouis G Castonguay, Larry E BeutlerHuman Mutation|January 1, 1993
Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the geneT Vulliamy, E Beutler, L LuzzattoHuman Genetics|May 10, 1977
Variants of galactose-1-phosphate uridyl transferase in the Greek populationsA Thomakos, E Beutler, G StamatoyannopoulosPageof 195