Low uptake of prenatal screening for Down syndrome in minority ethnic groups and socially deprived groups: a reflection of women's attitudes or a failure to facilitate informed choices?

Author:

Dormandy Elizabeth,Michie Susan,Hooper Richard,Marteau Theresa M

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Epidemiology

Reference33 articles.

1. Andrews L, Fullarton J, Holtzman N, Motulsky A. Assessing Genetic Risks: Implications for health and social policy. In: Andrews L, Fullarton J, Holtzman N, Motulsky A (eds). Washington DC: National Academy Press, 1994.

2. General Medical Council. Seeking Patients' Consent: The Ethical Considerations. London: General Medical Council, 1999.

3. National Screening Committee. Second Report of the UK National Screening Committee. London: Department of Health, 2000.

4. Marteau TM, Dormandy E. Facilitating informed choice in prenatal testing: How well are we doing? Am J Med Genet2001;106:185–190.

5. Chilaka V, Konje J, Stewart C, Narayan H, Taylor D. Knowledge of Down syndrome in pregnant women from different ethnic groups. Prenat Diagn2001;21:159–164.

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