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Large numbers of genetic variants considered to be pathogenic are common in asymptomatic individuals
It is now affordable to order clinically interpreted whole genome sequence reports from clinical laboratories. One major component of these reports is derived from the knowledge base of previously identified pathogenic variants, including research articles, locus specific and other databases. While...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3786140/ https://ncbi.nlm.nih.gov/pubmed/23818451 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.22375 |
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