Patients' Rights to Laboratory Data: Trinucleotide Repeat Length in Huntington Disease
American Journal of Medical Genetics. 1996 Mar 1; 62(1): 6-9.
Autonomy; Beneficence; Counseling; Decision Making; Diagnosis; Disclosure; Disease; Genetic Counseling; Genetic Information; Genetic Screening; Huntington Disease; Institutional Policies; Laboratories; Paternalism; Patient Participation; Patients; Patients' Rights; Rights; Risks and Benefits; Trust; Truth Disclosure;
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