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K E Ormond

Showing results (1-10 of 13) with videos related to

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Journal of Genetic Counseling|July 5, 2015
Update and Review: Maternal Serum ScreeningK E Ormond
Journal of Genetic Counseling|November 16, 2013
Pre-screening education in multiple marker screening programs: The effect on patient anxiety and knowledgeK E Ormond, E Pergament, B A Fine
Quality Management in Health Care|August 18, 2000
The impact of genetic technologies on perceptions of disabilityK L Kirschner, K E Ormond, C J Gill
Journal of Community Genetics|December 23, 2021
Correction to: Treatment decision‑making in sickle cell disease patientsA Booth, V Bonham, M Porteus, et al.
Journal of Community Genetics|November 4, 2021
Treatment decision-making in sickle cell disease patientsA Booth, V Bonham, M Porteus, et al.
Journal of Genetic Counseling|February 10, 2006
Knowledge and attitudes toward a free education and Ashkenazi Jewish carrier testing programG Hegwer, C Fairley, J Charrow, et al.
Journal of Personalized Medicine|January 7, 2015
Attitudes towards Social Networking and Sharing Behaviors among Consumers of Direct-to-Consumer Personal GenomicsSandra Soo-Jin Lee, Simone L Vernez, K E Ormond, et al.
Patient Education and Counseling|November 18, 2008
Information preferences of high literacy pregnant women regarding informed consent models for genetic carrier screeningK E Ormond, S Banuvar, A Daly, et al.
Journal of Genetic Counseling|July 5, 2015
Recommendations for Telephone CounselingK E Ormond, J Haun, L Cook, et al.
Journal of Genetic Counseling|May 12, 2007
What do patients prefer: informed consent models for genetic carrier testingK E Ormond, M Iris, S Banuvar, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Journal of Genetic Counseling|July 5, 2015
Update and Review: Maternal Serum ScreeningK E Ormond
Journal of Genetic Counseling|November 16, 2013
Pre-screening education in multiple marker screening programs: The effect on patient anxiety and knowledgeK E Ormond, E Pergament, B A Fine
Quality Management in Health Care|August 18, 2000
The impact of genetic technologies on perceptions of disabilityK L Kirschner, K E Ormond, C J Gill
Journal of Community Genetics|December 23, 2021
Correction to: Treatment decision‑making in sickle cell disease patientsA Booth, V Bonham, M Porteus, et al.
Journal of Community Genetics|November 4, 2021
Treatment decision-making in sickle cell disease patientsA Booth, V Bonham, M Porteus, et al.
Journal of Genetic Counseling|February 10, 2006
Knowledge and attitudes toward a free education and Ashkenazi Jewish carrier testing programG Hegwer, C Fairley, J Charrow, et al.
Journal of Personalized Medicine|January 7, 2015
Attitudes towards Social Networking and Sharing Behaviors among Consumers of Direct-to-Consumer Personal GenomicsSandra Soo-Jin Lee, Simone L Vernez, K E Ormond, et al.
Patient Education and Counseling|November 18, 2008
Information preferences of high literacy pregnant women regarding informed consent models for genetic carrier screeningK E Ormond, S Banuvar, A Daly, et al.
Journal of Genetic Counseling|July 5, 2015
Recommendations for Telephone CounselingK E Ormond, J Haun, L Cook, et al.
Journal of Genetic Counseling|May 12, 2007
What do patients prefer: informed consent models for genetic carrier testingK E Ormond, M Iris, S Banuvar, et al.
Pageof 2