Reply to Ross' commentary: Reproductive benefit through newborn screening: preferences, policy and ethics
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/ejhg201225.pdf
Reference20 articles.
1. Bombard Y, Miller FA, Hayeems RZ et al: Health-care providers' views on pursuing reproductive benefit through newborn screening: the case of sickle cell disorders. Eur J Hum Genet 2011; 20: 498–504.
2. Ross LF : Newborn screening for sickle cell disease: whose reproductive benefit? Eur J Hum Genet 2011; 20: 484–485.
3. Health Council of the Netherlands: Screening: Between Hope and Hype. Hague: Health Council of the Netherlands, 2008.
4. Bailey Jr DB, Skinner D, Warren SF : Newborn screening for developmental disabilities: reframing presumptive benefit. Am J Public Health 2005; 95: 1889–1893.
5. Bailey DBJ, Beskow LM, Davis AM, Skinner D : Changing perspectives on the benefits of newborn screening. Ment Retard Dev Disabil 2006; 12: 10.
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1. Decision-Making About Newborn Screening Panels in Canada: Risk Management and Public Participation;Democratizing Risk Governance;2023
2. SPATIAL DISTRIBUTION OF NEWBORNS WITH SICKLE CELL TRAIT IN SERGIPE, BRAZIL;Revista Paulista de Pediatria;2020
3. Fostering caring relationships: Suggestions to rethink liberal perspectives on the ethics of newborn screening;Bioethics;2018-02-14
4. Benefits and burdens of newborn screening: public understanding and decision-making;Personalized Medicine;2014-08
5. Defining the Scope of Public Engagement: Examining the “Right Not to Know” in Public Health Genomics;Journal of Law, Medicine & Ethics;2014
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