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Your search keyword '"Dizjikan, Farid Yavari"' showing total 12 results

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

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

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

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

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

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

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

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

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

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

12. An interconnected data infrastructure to support large-scale rare disease research.

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