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Frontiers in Genetics|June 17, 2022
Developing a National Newborn Genomes Program: An Approach Driven by Ethics, Engagement and Co-designAmanda Pichini, Arzoo Ahmed, Christine Patch, et al.
European Journal of Human Genetics : EJHG|June 21, 2012
Developing a policy for paediatric biobanks: principles for good practiceKristien Hens, Carla E Van El, Pascal Borry, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and CounsellorsAnna Middleton, Peter Marks, Anita Bruce, et al.
Wellcome Open Research|February 15, 2020
Potential for diagnosis of infectious disease from the 100,000 Genomes Project Metagenomic Dataset: Recommendations for reporting resultsGkikas Magiorkinis, Philippa C Matthews, Susan E Wallace, et al.
European Journal of Human Genetics : EJHG|September 22, 2016
Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disordersKate Wolfe, André Strydom, Deborah Morrogh, et al.
HGG Advances|October 23, 2023
The legacy of language: What we say, and what people hear, when we talk about genomicsAnna Middleton, Alessia Costa, Richard Milne, et al.
Plos One|November 8, 2021
Return of individual research results from genomic research: A systematic review of stakeholder perspectivesDanya F Vears, Joel T Minion, Stephanie J Roberts, et al.
Open Research Europe|April 11, 2025
Genomic findings with familial implications: agenda setting in light of mainstreamingAmicia Phillips, Eva Van Steijvoort, Maria Siermann, et al.
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