Routes to expanded carrier screening in the UK: the perspectives of professional stakeholders
Parental Decision Making Regarding Level of Newborn Screening Participation in the Homebirth Setting
“Would you want to know?” Questions of utility and responsibility in Italian laypersons’ preferences about genetic risk communication
The Effect of Sample Type on Genetic Testing Completion in Pediatric Congenital Hearing Loss Patients
Re-Consent Practices in Biobanks in Japan: Current Status and Stakeholder Perspectives
Genetic Testing for Cystic Fibrosis in South Africa: A 10-Year Retrospective Study
Scoping review: The current landscape of NIPT in South Africa
Perceptions of Family Health History in an East Baltimore Community
Lack of Provision of Social and Emotional Information about Down Syndrome Associated with Negative Prenatal Diagnosis Experiences
Genetic Counselling for Psychiatric Conditions: exploring current perceptions of family physicians and psychiatrist in Portugal