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Pediatrics|February 13, 2013
Disclosure of incidental findings from next-generation sequencing in pediatric genomic researchRuqayyah Abdul-Karim, Benjamin E Berkman, David Wendler, et al.Obstetrics and Gynecology|February 12, 2019
Noninvasive Prenatal Whole Genome Sequencing: Pregnant Women's Views and PreferencesHaley K Sullivan, Michelle Bayefsky, Paul G Wakim, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 30, 2021
Exploring the motivations of research participants who chose not to learn medically actionable secondary genetic findings about themselvesWill Schupmann, Skye A Miner, Haley K Sullivan, et al.Prenatal Diagnosis|January 15, 2025
Comparing the Introduction and Implementation of Noninvasive Prenatal Testing (NIPT) in Japan, the Netherlands, and the United States: An Integrative ReviewChloe Connor, Taisuke Sato, Diana W Bianchi, et al.Prenatal Diagnosis|December 9, 2023
Precarious hope: Ethical considerations for offering experimental fetal therapies outside of research after initial studies in humansSaskia Hendriks, Janyne Althaus, Meredith A Atkinson, et al.Journal of Medical Ethics|June 16, 2018
Development of a consensus approach for return of pathology incidental findings in the Genotype-Tissue Expression (GTEx) projectNicole C Lockhart, Carol J Weil, Latarsha J Carithers, et al.American Journal of Human Genetics|July 4, 2015
Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and AdolescentsJeffrey R Botkin, John W Belmont, Jonathan S Berg, et al.Pediatrics|May 16, 2012
Incidental medical information in whole-exome sequencingBenjamin D Solomon, Donald W Hadley, Daniel E Pineda-Alvarez, et al.Pageof 5