All Stories

  1. Analysis of the Phenotypes in the Rett Networked Database
  2. Dimensions of responsibility in medical genetics: exploring the complexity of the “duty to recontact”
  3. Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences
  4. Communication of Information about Genetic Risks: Putting Families at the Center
  5. Depression in Rett Syndrome
  6. Accounts of consent: Orienting to self-other relations regarding motivations to participate in cancer bio-banking