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Volumn 2, Issue 2, 1996, Pages 28-38
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Predictive and carrier testing of children: professional dilemmas for clinical geneticists.
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
AGE;
ARTICLE;
ATTITUDE;
CASE REPORT;
CHILD;
CHROMOSOME ABERRATION;
CHROMOSOME DISORDER;
DECISION MAKING;
EMPIRICAL APPROACH;
GENETIC COUNSELING;
GENETIC DISORDER;
GENETIC PREDISPOSITION;
GENETIC SCREENING;
GENETICS AND REPRODUCTION;
HETEROZYGOTE;
HUMAN;
INTERPERSONAL COMMUNICATION;
MOTIVATION;
NEOPLASM;
NEUROMUSCULAR DISEASE;
ONSET AGE;
PARENT;
PROBABILITY;
RISK;
RISK ASSESSMENT;
UNCERTAINTY;
UNITED KINGDOM;
EMPIRICAL APPROACH;
GENETICS AND REPRODUCTION;
AGE FACTORS;
AGE OF ONSET;
ATTITUDE;
CHILD;
CHROMOSOME ABERRATIONS;
CHROMOSOME DISORDERS;
DECISION MAKING;
GENETIC COUNSELING;
GENETIC DISEASES, INBORN;
GENETIC PREDISPOSITION TO DISEASE;
GENETIC SCREENING;
GREAT BRITAIN;
HETEROZYGOTE;
HUMANS;
MOTIVATION;
NEOPLASMS;
NEUROMUSCULAR DISEASES;
PARENTS;
PROBABILITY;
RISK;
RISK ASSESSMENT;
TRUTH DISCLOSURE;
UNCERTAINTY;
MLCS;
MLOWN;
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EID: 0030348208
PISSN: 10239022
EISSN: None
Source Type: Journal
DOI: 10.1179/hrge.2.2.u5741641357jtu7h Document Type: Article |
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Times cited : (12)
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References (0)
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