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Nurs Stand ; 20(3): 48-51, 2005.
Article in English | MEDLINE | ID: mdl-16223195

ABSTRACT

This article discusses the rights of patients in relation to types of genetic tests and the broader implications for families. Use and misuse of genetic information is considered, including scenarios and points to consider. The use of a non-directive approach in genetic counselling is emphasised and multifactorial disorders, prenatal diagnosis and learning disabilities are discussed.


Subject(s)
Genetic Testing , Genetic Counseling/ethics , Genetic Testing/ethics , Human Rights , Humans , Informed Consent/ethics
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