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	21.	A Knotty Problem of Intertwined Rights. [electronic resource] by McKinney, Ross E Producer: 20160503 In: The American journal of bioethics : AJOB vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	The emergence of an ethical duty to disclose genetic research results: international perspectives. [electronic resource] by Knoppers, Bartha Maria Joly, Yann Simard, Jacques Durocher, Francine Producer: 20070103 In: European journal of human genetics : EJHG vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Is it ethical to deny genetic research participants individualised results? [electronic resource] by Affleck, P Producer: 20091014 In: Journal of medical ethics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Ethics in population-based genetic research. [electronic resource] by DeCamp, Matthew Sugarman, Jeremy Producer: 20041026 In: Accountability in research vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics. [electronic resource] by Carrieri, Daniele Howard, Heidi C Benjamin, Caroline Clarke, Angus J Dheensa, Sandi Doheny, Shane Hawkins, Naomi Halbersma-Konings, Tanya F Jackson, Leigh Kayserili, Hülya Kelly, Susan E Lucassen, Anneke M Mendes, Álvaro Rial-Sebbag, Emmanuelle Stefánsdóttir, Vigdís Turnpenny, Peter D van El, Carla G van Langen, Irene M Cornel, Martina C Forzano, Francesca Producer: 20190509 In: European journal of human genetics : EJHG vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Failing to refer or follow up patients. [electronic resource] by Panting, Gerard Producer: 20051025 In: East African medical journal vol. 82 Availability: No items available. Save to lists Add to cart (remove)
	27.	When do genetic researchers have a duty to recontact study participants? [electronic resource] by Wade, Christopher H Kalfoglou, Andrea L Producer: 20070130 In: The American journal of bioethics : AJOB vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Taking our obligations to research participants seriously: disclosing individual results of genetic research. [electronic resource] by Manolio, Teri A Producer: 20070130 In: The American journal of bioethics : AJOB vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe. [electronic resource] by Sirchia, Fabio Carrieri, Daniele Dheensa, Sandi Benjamin, Caroline Kayserili, Hülya Cordier, Christophe van El, Carla G Turnpenny, Peter D Melegh, Bela Mendes, Álvaro Halbersma-Konings, Tanya F van Langen, Irene M Lucassen, Anneke M Clarke, Angus J Forzano, Francesca Kelly, Susan E Producer: 20190221 In: European journal of human genetics : EJHG vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	The search for clarity in communicating research results to study participants. [electronic resource] by Shalowitz, D I Miller, F G Producer: 20081124 In: Journal of medical ethics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Disclosing genetic research results: examples from practice. [electronic resource] by Ormond, Kelly E Producer: 20070130 In: The American journal of bioethics : AJOB vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Follow-up of patients with colorectal cancer: the evidence is in favour but we are still in need of a protocol. [electronic resource] by Papagrigoriadis, Savvas Producer: 20070515 In: International journal of surgery (London, England) vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	DNA databanks and consent: a suggested policy option involving an authorization model. [electronic resource] by Caulfield, Timothy Upshur, Ross E G Daar, Abdallah Producer: 20040811 In: BMC medical ethics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Primary lower urinary tract reconstruction for nonfunctioning renal moieties associated with obstructing ureteroceles. [electronic resource] by Gran, Christopher D Kropp, Bradley P Cheng, Earl Y Kropp, Kenneth A Producer: 20050113 In: The Journal of urology vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature. [electronic resource] by Otten, Ellen Plantinga, Mirjam Birnie, Erwin Verkerk, Marian A Lucassen, Anneke M Ranchor, Adelita V Van Langen, Irene M Producer: 20160601 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Recontacting in clinical practice: an investigation of the views of healthcare professionals and clinical scientists in the United Kingdom. [electronic resource] by Carrieri, Daniele Dheensa, Sandi Doheny, Shane Clarke, Angus J Turnpenny, Peter D Lucassen, Anneke M Kelly, Susan E Producer: 20170807 In: European journal of human genetics : EJHG vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Re-contact to advise of testing available to detect high risk for carcinoma: response to letters sent to persons initially ascertained for other genetic reasons. [electronic resource] by Swiglo, B A Lebel, R R Producer: 19990218 In: American journal of human genetics vol. 61 Availability: No items available. Save to lists Add to cart (remove)
	38.	Feedback of Individual Genetic Results to Research Participants: Is It Feasible in Europe? [electronic resource] by Budin-Ljøsne, Isabelle Mascalzoni, Deborah Soini, Sirpa Machado, Helena Kaye, Jane Bentzen, Heidi Beate Rial-Sebbag, Emmanuelle D'Abramo, Flavio Witt, Michał Schamps, Geneviève Katić, Višnja Krajnovic, Dusanca Harris, Jennifer R Producer: 20170116 In: Biopreservation and biobanking vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	Recontacting patients for multigene panel testing in hereditary cancer: Efficacy and insights. [electronic resource] by Sawyer, Lindsey Creswick, Heather Lewandowski, Raymond Quillin, John Producer: 20200731 In: Journal of genetic counseling vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	The duty to recontact: benefit and harm. [electronic resource] by Sharpe, N F Producer: 20001002 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 124 results.