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Familial Cancer|March 23, 2020
Genetic health professionals' experiences with initiating reanalysis of genomic sequence dataDanya F Vears, Karine Sénécal, Pascal Borry
European Journal of Medical Genetics|August 5, 2017
Reporting practices for variants of uncertain significance from next generation sequencing technologiesDanya F Vears, Karine Sénécal, Pascal Borry
European Journal of Medical Genetics|September 1, 2019
Exploration of genetic health professional - laboratory specialist interactions in diagnostic genomic sequencingDanya F Vears, Karine Sénécal, Pascal Borry
The Journal of Medicine and Philosophy|January 17, 2020
On the Epistemic Status of Prenatal Ultrasound: Are Ultrasound Scans Photographic Pictures?Maddalena Favaretto, Danya F Vears, Pascal Borry
Personalized Medicine|March 11, 2020
'It's much more grey than black and white': clinical geneticists' views on the oversight of consumer genomics in EuropeLouiza Kalokairinou, Pascal Borry, Heidi C Howard
Personalized Medicine|May 23, 2018
Letter to the EditorRyan Phelan, Pascal Borry, Heidi C Howard
Journal of Medical Genetics|July 24, 2017
Regulating the advertising of genetic tests in Europe: a balancing actLouiza Kalokairinou, Pascal Borry, Heidi Carmen Howard
Bioethics|April 3, 2009
'Nobody tosses a dwarf!' The relation between the empirical and the normative reexaminedCarlo Leget, Pascal Borry, Raymond de Vries
Best Practice & Research. Clinical Obstetrics & Gynaecology|March 18, 2017
Growing complexity of (expanded) carrier screening: Direct-to-consumer, physician-mediated, and clinic-based offersDavit Chokoshvili, Danya F Vears, Pascal Borry
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