Children and biobanks: a review of the ethical and legal discussion
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00439-011-1031-8.pdf
Reference56 articles.
1. (1989) United Nations Convention on the Rights of the Child
2. Ashcroft R, Goodenough T, Williamson E, Kent J (2003) Children’s consent to research participation: social context and personal experience in validate fixed cutoff rules. Am J Bioeth 3:16–18
3. Berrington JE, Snowdon C, Fenton AC (2010) Parents’ attitudes to neonatal research involving venepuncture. Clin Ethics 5:148–155
4. Brothers KB (2011) Biobanking in pediatrics: the human nonsubjects approach. Per Med 8(1):71–79
5. Brothers KB, Clayton EW (2009) Biobanks: too long to wait for consent. Science 326:798
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4. Paediatric biobanking for health: The ethical, legal, and societal landscape;Frontiers in Public Health;2022-09-27
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