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Publication
Defining critical educational components of informed consent for genetic testing: Views of US-based genetic counselors and medical geneticists
European Journal of Human Genetics -
Publication
Direct notification by health professionals of relatives at-risk of genetic conditions (with patient consent): Views of the Australian public
European Journal of Human Genetics -
Publication
What matters to parents? A scoping review of parents’ service experiences and needs regarding genetic testing for rare diseases
European Journal of Human Genetics -
Publication
The future is mainstream: Genetic counselling should be embedded in mainstream medicine
European Journal of Human Genetics -
Publication
Consanguineous couples’ experiences and views regarding expanded carrier screening: Barriers and facilitators in the decision-making process
European Journal of Human Genetics -
Publication
Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing
European Journal of Human Genetics -
Publication
Searching for a sense of closure: Parental experiences of recontacting after a terminated pregnancy for congenital malformations
European Journal of Human Genetics -
Publication
Antiracist structural intervention at the Emory University Institutional Review Board
Ethics & Human Research -
Publication
Contributing to the on-going debate around the clinical application of preimplantation embryo selection based on polygenic risk scores (PGT-P)
European Journal of Human Genetics -
Publication
Future pHealth ecosystem-holistic view on privacy and trust
Journal of Personalized Medicine