The Privacy Implications of Professor Anderson's Proposed Mandatory Registry for Bone Marrow Donation: A Reply
Hartman, Rhonda G.
University of Pittsburgh Law Review. 1993 Winter; 54(2): 531-551.
Altruism; Autonomy; Blood; Blood Specimen Collection; Bone Marrow; Coercion; Common Good; Constitutional Law; Decision Making; Donors; Due Process; Data Banks; Federal Government; Freedom; Government; Injuries; Law; Legal Rights; Mandatory Programs; Privacy; Public Policy; Random Selection; Registries; Rights; Risk; Scarcity; Specimen Collection; State Government; State Interest; Supreme Court Decisions; Tissue Donation; Voluntary Programs;
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