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Volumn 83, Issue 5, 1996, Pages 307-314
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The Human Genome Project and the clinician.
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Author keywords
[No Author keywords available]
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Indexed keywords
ARTICLE;
BIOTECHNOLOGY;
CONFIDENTIALITY;
COST BENEFIT ANALYSIS;
DUTY TO RECONTACT;
FORECASTING;
GENERAL PRACTICE;
GENETIC DISORDER;
GENETIC PRIVACY;
GENETIC PROCEDURES;
GENETIC SCREENING;
GENETICS;
GENETICS AND REPRODUCTION;
GOVERNMENT REGULATION;
HUMAN;
HUMAN GENOME PROJECT;
INFORMED CONSENT;
INTERPERSONAL COMMUNICATION;
LEGAL APPROACH;
LEGAL ASPECT;
MEDICAL RECORD;
PATE V. THRELKEL;
PATIENT REFERRAL;
PHYSICIAN;
GENETICS AND REPRODUCTION;
HUMAN GENOME PROJECT;
LEGAL APPROACH;
PATE V. THRELKEL;
BIOTECHNOLOGY;
CONFIDENTIALITY;
COST-BENEFIT ANALYSIS;
DISCLOSURE;
DUTY TO RECONTACT;
DUTY TO WARN;
FAMILY PRACTICE;
FORECASTING;
GENETIC DISEASES, INBORN;
GENETIC PRIVACY;
GENETIC SCREENING;
GENETIC TECHNIQUES;
GOVERNMENT REGULATION;
HUMAN GENOME PROJECT;
HUMANS;
INFORMED CONSENT;
MEDICAL RECORDS;
PHYSICIANS;
REFERRAL AND CONSULTATION;
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EID: 0030138818
PISSN: 00154148
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (7)
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References (0)
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