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From the Blood Systems Research Institute, San Francisco, California; the Pharmaceutical Outcomes Research and Policy Program, University of Washington, Seattle, Washington; the Department of Laboratory Medicine, University of California at San Francisco, San Francisco, California; Blood Systems, Inc., Scottsdale, Arizona; the Department of Epidemiology and Biostatistics, University of California Berkeley, Berkeley, California; and Creative Testing Solutions, Tempe, Arizona.
From the Blood Systems Research Institute, San Francisco, California; the Pharmaceutical Outcomes Research and Policy Program, University of Washington, Seattle, Washington; the Department of Laboratory Medicine, University of California at San Francisco, San Francisco, California; Blood Systems, Inc., Scottsdale, Arizona; the Department of Epidemiology and Biostatistics, University of California Berkeley, Berkeley, California; and Creative Testing Solutions, Tempe, Arizona.
From the Blood Systems Research Institute, San Francisco, California; the Pharmaceutical Outcomes Research and Policy Program, University of Washington, Seattle, Washington; the Department of Laboratory Medicine, University of California at San Francisco, San Francisco, California; Blood Systems, Inc., Scottsdale, Arizona; the Department of Epidemiology and Biostatistics, University of California Berkeley, Berkeley, California; and Creative Testing Solutions, Tempe, Arizona.
From the Blood Systems Research Institute, San Francisco, California; the Pharmaceutical Outcomes Research and Policy Program, University of Washington, Seattle, Washington; the Department of Laboratory Medicine, University of California at San Francisco, San Francisco, California; Blood Systems, Inc., Scottsdale, Arizona; the Department of Epidemiology and Biostatistics, University of California Berkeley, Berkeley, California; and Creative Testing Solutions, Tempe, Arizona.
From the Blood Systems Research Institute, San Francisco, California; the Pharmaceutical Outcomes Research and Policy Program, University of Washington, Seattle, Washington; the Department of Laboratory Medicine, University of California at San Francisco, San Francisco, California; Blood Systems, Inc., Scottsdale, Arizona; the Department of Epidemiology and Biostatistics, University of California Berkeley, Berkeley, California; and Creative Testing Solutions, Tempe, Arizona.
From the Blood Systems Research Institute, San Francisco, California; the Pharmaceutical Outcomes Research and Policy Program, University of Washington, Seattle, Washington; the Department of Laboratory Medicine, University of California at San Francisco, San Francisco, California; Blood Systems, Inc., Scottsdale, Arizona; the Department of Epidemiology and Biostatistics, University of California Berkeley, Berkeley, California; and Creative Testing Solutions, Tempe, Arizona.
From the Blood Systems Research Institute, San Francisco, California; the Pharmaceutical Outcomes Research and Policy Program, University of Washington, Seattle, Washington; the Department of Laboratory Medicine, University of California at San Francisco, San Francisco, California; Blood Systems, Inc., Scottsdale, Arizona; the Department of Epidemiology and Biostatistics, University of California Berkeley, Berkeley, California; and Creative Testing Solutions, Tempe, Arizona.
From the Blood Systems Research Institute, San Francisco, California; the Pharmaceutical Outcomes Research and Policy Program, University of Washington, Seattle, Washington; the Department of Laboratory Medicine, University of California at San Francisco, San Francisco, California; Blood Systems, Inc., Scottsdale, Arizona; the Department of Epidemiology and Biostatistics, University of California Berkeley, Berkeley, California; and Creative Testing Solutions, Tempe, Arizona.
From the Blood Systems Research Institute, San Francisco, California; the Pharmaceutical Outcomes Research and Policy Program, University of Washington, Seattle, Washington; the Department of Laboratory Medicine, University of California at San Francisco, San Francisco, California; Blood Systems, Inc., Scottsdale, Arizona; the Department of Epidemiology and Biostatistics, University of California Berkeley, Berkeley, California; and Creative Testing Solutions, Tempe, Arizona.
From the Blood Systems Research Institute, San Francisco, California; the Pharmaceutical Outcomes Research and Policy Program, University of Washington, Seattle, Washington; the Department of Laboratory Medicine, University of California at San Francisco, San Francisco, California; Blood Systems, Inc., Scottsdale, Arizona; the Department of Epidemiology and Biostatistics, University of California Berkeley, Berkeley, California; and Creative Testing Solutions, Tempe, Arizona.