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Seminars in Fetal & Neonatal Medicine
Volume 13, Issue 2
, Pages 99-102
, April 2008
Cultural variation in values attached to informed choice in the context of prenatal diagnosis
References
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- . Challenging the bioethical application of the autonomy principle within multicultural societies. J Appl Philos. 2004;21:15–31
- . Informed choice in the Pakistani milieu: the physicians' perspective. J Med Ethics. 2005;31:93–96
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- . Informed choice in screening programmes: do leaflets help? A critical literature review. J Public Health. 2006;28(4):309–317
- . An assessment of written patient information provided at the egentic clinic and relating to genetic testing in seven European countries. Eur J Hum Genet. 2007;1–11
- . Undergoing prenatal screening for Down's syndrome: presentation of choice and information in Europe and Asia. Eur J Hum Genet. 2007;15:563–569
- Van den Heuvel A, Hollywood A, Hogg J, et al. Informed choice to undergo prenatal screening for thalassaemia: a description of written information given to pregnant women in Europe and beyond. Prenat Diagn, submitted for publication.
- Information needs and decisional preferences in women with breast cancer. J Am Med Assoc. 1997;277:1485–1492
- Attitudes towards genetic diagnosis in Pakistan: a survey of medical and legal communities and parents of thalassemic children. Community Genet. 2007;10:140–146
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- . The role of doctor's opinion in shared decision making: what does shared decision making really mean when considering invasive medical procedures?. Health Expect. 2005;8:97–102
PII: S1744-165X(07)00156-4
doi: 10.1016/j.siny.2007.12.010
© 2008 Elsevier Ltd. All rights reserved.
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Seminars in Fetal & Neonatal Medicine
Volume 13, Issue 2
, Pages 99-102
, April 2008
