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Volumn 147, Issue 3 SUPPL., 2005, Pages
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Implementation of informed consent for a cystic fibrosis newborn screening program in France: Low refusal rates for optional testing
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Author keywords
[No Author keywords available]
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Indexed keywords
CONFERENCE PAPER;
CYSTIC FIBROSIS;
FRANCE;
GENETIC COUNSELING;
GENETIC SCREENING;
HEALTH PROGRAM;
HUMAN;
INFORMED CONSENT;
MEDICAL ETHICS;
NEWBORN;
NEWBORN SCREENING;
PARENTAL CONSENT;
PATIENT ABANDONMENT;
PATIENT COMPLIANCE;
PATIENT EDUCATION;
PRIORITY JOURNAL;
ALGORITHMS;
ATTITUDE TO HEALTH;
CONSENT FORMS;
CYSTIC FIBROSIS;
DNA MUTATIONAL ANALYSIS;
DOCUMENTATION;
FRANCE;
GENETIC COUNSELING;
GENETIC PRIVACY;
HEALTH EDUCATION;
HUMANS;
IMMUNOASSAY;
INFANT, NEWBORN;
NEONATAL SCREENING;
PARENTAL CONSENT;
PARENTS;
REFUSAL TO PARTICIPATE;
TEACHING MATERIALS;
TRYPSINOGEN;
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EID: 25844512634
PISSN: 00223476
EISSN: None
Source Type: Journal
DOI: 10.1016/j.jpeds.2005.08.008 Document Type: Conference Paper |
Times cited : (24)
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References (8)
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