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Your search keyword '"Bros-Facer, Virginie"' showing total 25 results

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25 results on '"Bros-Facer, Virginie"'

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1. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

2. Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a Treatabolome

4. A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome

5. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

6. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

7. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

8. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

10. Solving unsolved rare neurological diseases-a Solve-RD viewpoint

11. The RD-connect genome-phenome analysis platform: accelerating diagnosis, research, and gene discovery for rare diseases

12. Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

13. The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases

14. The Treatabolome Database and Platform: enhancing Rare Diseases’ treatment visibility

15. A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity

16. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

17. Correction: Solving unsolved rare neurological diseases : A Solve-RD viewpoint

18. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

19. Meeting Patients' Right to the Correct Diagnosis : Ongoing International Initiatives on Undiagnosed Rare Diseases and Ethical and Social Issues

20. Recommendations for Improving the Quality of Rare Disease Registries

22. Recommendations for Improving the Quality of Rare Disease Registries

24. A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity

25. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

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