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Open Peer Commentaries

Prenatal Whole Genome Sequencing: An Argument for Professional Self-Regulation

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Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (3)

Kelsey Mumford, Nina Roesner & Benjamin E. Berkman. (2023) The Potential Role of Nudging in Expanded Noninvasive Prenatal Testing. The American Journal of Bioethics 23:3, pages 61-63.
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Michelle J. Bayefsky & Benjamin E. Berkman. (2022) Implementing Expanded Prenatal Genetic Testing: Should Parents Have Access to Any and All Fetal Genetic Information?. The American Journal of Bioethics 22:2, pages 4-22.
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Articles from other publishers (7)

Dagmar Schmitz & Wolfram Henn. (2021) The fetus in the age of the genome. Human Genetics 141:5, pages 1017-1026.
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Dagmar Schmitz & Marcus Düwell. (2021) Die Rechte zukünftiger Kinder im Kontext pränataler DiagnostikThe rights of future children in the context of prenatal testing. Ethik in der Medizin 34:1, pages 49-63.
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Hazar Haidar & Renata Iskander. (2022) Non-invasive Prenatal Testing for Fetal Whole Genome Sequencing: An Interpretive Critical Review of the Ethical, Legal, Social, and Policy Implications. Canadian Journal of Bioethics 5:1, pages 1.
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Min Chen, Jingsi Chen, Chunli Wang, Fei Chen, Yinong Xie, Yufan Li, Nan Li, Jing Wang, Victor Wei Zhang & Dunjin Chen. (2020) Clinical application of medical exome sequencing for prenatal diagnosis of fetal structural anomalies. European Journal of Obstetrics & Gynecology and Reproductive Biology 251, pages 119-124.
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Greg Stapleton, Wybo Dondorp, Peter Schröder-Bäck & Guido de Wert. (2019) Just choice: a Danielsian analysis of the aims and scope of prenatal screening for fetal abnormalities. Medicine, Health Care and Philosophy 22:4, pages 545-555.
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Bobbi Fleiss, Flora Wong, Fiona Brownfoot, Isabelle K. Shearer, Olivier Baud, David W. Walker, Pierre Gressens & Mary Tolcos. (2019) Knowledge Gaps and Emerging Research Areas in Intrauterine Growth Restriction-Associated Brain Injury. Frontiers in Endocrinology 10.
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M.C. de Wit, E.M. Bunnik, A.T.J.I. Go, I.D. de Beaufort, R.M.W. Hofstra, E.A.P. Steegers & R.J.H. Galjaard. (2017) Amniocentesis is still the best option for advanced genomic testing in case of fetal malformations. Prenatal Diagnosis 37:13, pages 1360-1363.
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