Ethical Considerations in the Social Context of Huntington Disease
Disease Markers. 1992 Jul-Aug; 10(4): 171-183.
Abortion; Autonomy; Beneficence; Case Studies; Coercion; Confidentiality; Counseling; Diagnosis; Disclosure; Disease; Family Members; Future Generations; Genetic Counseling; Genetic Research; Guidelines; Genetic Screening; Health; Huntington Disease; Justice; Late-Onset Disorders; Normality; Obligations of Society; Obligations to Society; Organizations; Paternalism; Patients; Pedigree; Prenatal Diagnosis; Professional Organizations; Reproduction; Research; Risk; Risks and Benefits; Selective Abortion; Self Concept;
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