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Your search keyword '"de Voer, R. M."' showing total 8 results

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8 results on '"de Voer, R. M."'

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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

3. Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

5. Evaluating the role of NTHL1 p.Q90* allele in inherited breast cancer predisposition

6. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related Autosomal Recessive Ectodermal Dysplasia 14

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

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

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