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Genetic Evidence and Integration of Various Data Sources for Classifying Uncertain Variants Into a Single Model
Genetic testing often results in the finding of a variant whose clinical significance is unknown. A number of different approaches have been employed in the attempt to classify such variants. For some variants, case-control, segregation, family history, or other statistical studies can provide stron...
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| Päätekijät: | , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2008
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2936773/ https://ncbi.nlm.nih.gov/pubmed/18951437 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.20897 |
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