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2. To disclose, or not to disclose? Context matters.

3. Public views on participating in newborn screening using genome sequencing.

5. Exploring resources for intrafamilial communication of cancer genetic risk: we still need to talk.

6. Personalized medicine and access to health care: potential for inequitable access?

7. Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?

8. Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening.

9. Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information.

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