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Archives of Medical Research|January 1, 1995
Molecular heterogeneity of G-6-PD deficiency in MexicoM D Medina, G Vaca, A Esparza, et al.
British Journal of Haematology|November 13, 2001
Human transferrin G277S mutation: a risk factor for iron deficiency anaemiaP L Lee, C Halloran, R Trevino, 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.
Transfusion|November 1, 1982
In vivo viability of red blood cells stored in CPDA-2P R Sohmer, G L Moore, E Beutler, et al.
Sleep|January 1, 1981
Differentiating psychological characteristics of patients with sleep apnea and narcolepsyL E Beutler, J C Ware, I Karacan, et al.
American Journal of Human Genetics|September 1, 1990
Molecular genetics of the glucose-6-phosphate dehydrogenase (G6PD) Mediterranean variant and description of a new G6PD mutant, G6PD Andalus1361AJ L Vives-Corrons, W Kuhl, M A Pujades, et al.
Blood|November 15, 1989
Molecular heterogeneity of glucose-6-phosphate dehydrogenase A-E Beutler, W Kuhl, J L Vives-Corrons, et al.
American Journal of Human Genetics|December 1, 1987
The human glucocerebrosidase gene has two functional ATG initiator codonsJ A Sorge, C West, W Kuhl, et al.
The American Psychologist|December 1, 1995
Bridging scientist and practitioner perspectives in clinical psychologyL E Beutler, R E Williams, P J Wakefield, et al.
The Journal of Pediatrics|August 1, 1997
Glucose-6-phosphate dehydrogenase Durham: a de novo mutation associated with chronic hemolytic anemiaS A Zimmerman, R E Ware, L Forman, et al.
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