Sickle cell screening policies as portent: how will the human genome project affect public sector genetic services?

Journal of the National Medical Association

Volumn 87, Issue 11, 1995, Pages 807-812

  Phoenix, D D ^a   Lybrook, S M ^a   Trottier, R W ^a   Hodgin, F C ^a   Crandall, L A ^a  

^a CLEMSON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CIVIL RIGHTS; GENETIC SCREENING; GENETICS; GENETICS AND REPRODUCTION; HEALTH CARE POLICY; HUMAN; HUMAN GENOME PROJECT; INTERPERSONAL COMMUNICATION; MEDICAL ETHICS; NEWBORN; ORGANIZATION AND MANAGEMENT; SICKLE CELL ANEMIA; UNITED STATES;

GENETICS AND REPRODUCTION;

ANEMIA, SICKLE CELL; CIVIL RIGHTS; ETHICS, MEDICAL; GENETIC SCREENING; GEORGIA; HEALTH POLICY; HUMAN GENOME PROJECT; HUMANS; INFANT, NEWBORN; TRUTH DISCLOSURE;

EID: 0029395813     PISSN: 00279684     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)