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5. Model consent clauses for rare disease research

6. An empirical analysis of the legal frameworks governing genetic services labs in Canadian provinces.

7. European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

8. The return of results of deceased research participants.

9. Differences in regulatory frameworks governing genetic laboratories in four countries.

10. L'encadrement legislatif de la vente directe des tests genetiques et le systeme de sante quebecois.

11. European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

12. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

13. Simplifying research access to genomics and health data with Library Cards

14. Epigenome-based cancer risk prediction: Rationale, opportunities and challenges

15. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

16. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

18. A comparative analysis of the requirements for the use of data in biobanks based in Finland, Germany, the Netherlands, Norway and the United Kingdom

20. Epigenome-based cancer risk prediction: rationale, opportunities and challenges

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