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Personalized Medicine|May 2, 2018
Noninvasive prenatal testing: a survey of young (future) parents in FlandersPascal Borry, Maddalena Favaretto, Ann Batthyany, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|November 4, 2014
Psychosocial impact of pediatric living-donor kidney and liver transplantation on recipients, donors, and the family: a systematic reviewKristof Thys, Karl-Leo Schwering, Marion Siebelink, et al.
European Journal of Human Genetics : EJHG|January 8, 2022
Informing relatives of their genetic risk: an examination of the Belgian legal contextAmicia Phillips, Thomas Bronselaer, Pascal Borry, et al.
European Journal of Human Genetics : EJHG|September 29, 2016
Registered access: a 'Triple-A' approachStephanie O M Dyke, Emily Kirby, Mahsa Shabani, et al.
Human Reproduction Update|February 27, 2020
Interest in expanded carrier screening among individuals and couples in the general population: systematic review of the literatureEva Van Steijvoort, Davit Chokoshvili, Jeffrey W Cannon, et al.
European Journal of Human Genetics : EJHG|January 29, 2015
Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmesHeidi Carmen Howard, Bartha Maria Knoppers, Martina C Cornel, et al.
Journal of Community Genetics|December 21, 2024
Healthcare professionals' experiences with expanded noninvasive prenatal screening: challenges and solutionsZoë Claesen-Bengtson, Karuna R M van der Meij, Joris R Vermeesch, et al.
Forensic Science International. Genetics|July 30, 2016
Biohistorical materials and contemporary privacy concerns-the forensic case of King Albert IMaarten H D Larmuseau, Bram Bekaert, Maarten Baumers, et al.
Human Reproduction (Oxford, England)|March 3, 2011
Preconceptional genetic carrier testing and the commercial offer directly-to-consumersPascal Borry, Lidewij Henneman, Phillis Lakeman, et al.
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