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Health, Risk & Society Volume 9, 2007 - Issue 1
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Original Articles

Maximizing the benefits and minimizing the risks associated with prenatal genetic testing

Merryn Ekberg Lecturer in Health Sociology The University of Northampton, UKCorrespondence[email protected]
Pages 67-81 | Published online: 01 Mar 2007

Citations (9)

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Read on this site (1)

Roxanne Parrott, Kathryn F. Peters & Tara Traeder. (2012) Uncertainty Management and Communication Preferences Related to Genetic Relativism Among Families Affected by Down Syndrome, Marfan Syndrome, and Neurofibromatosis. Health Communication 27:7, pages 663-671.
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Articles from other publishers (8)

Ruth M. Farrell, Madelyn Pierce, Christina Collart, Caitlin Craighead, Marissa Coleridge, Edward K. Chien, Uma Perni, Richard Frankel, Angela Ranzini, Brownsyne Tucker Edmonds & Susannah S. Rose. (2021) The impact of the emergence of COVID‐19 on women's prenatal genetic testing decisions. Prenatal Diagnosis 41:8, pages 1009-1017.
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Robin L. Page, Christina Murphey, Yahyahan Aras, Lei‐Shih Chen & Ryan Loftin. (2021) Pregnant Hispanic women's views and knowledge of prenatal genetic testing. Journal of Genetic Counseling 30:3, pages 838-848.
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Jon Leefmann, Manuel Schaper & Silke Schicktanz. (2017) The Concept of “Genetic Responsibility” and Its Meanings: A Systematic Review of Qualitative Medical Sociology Literature. Frontiers in Sociology 1.
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Hanna Rennert & Debra G. B. Leonard. 2016. Molecular Pathology in Clinical Practice. Molecular Pathology in Clinical Practice 945 973 .
Rebecca L. Walker & Clair Morrissey. (2012) Charting ELSI’s future course: lessons from the recent past. Genetics in Medicine 14:2, pages 259-267.
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Kelly Raspberry & Debra Skinner. (2010) Enacting genetic responsibility: experiences of mothers who carry the fragile X gene. Sociology of Health & Illness 33:3, pages 420-433.
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Janet L McCabe & Dave Holmes. (2011) Reversing Kristeva’s first instance of abjection: the formation of self reconsidered. Nursing Inquiry 18:1, pages 77-83.
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Susan E. Kelly. (2009) Choosing not to choose: reproductive responses of parents of children with genetic conditions or impairments. Sociology of Health & Illness 31:1, pages 81-97.
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