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A curated gene list for reporting results of newborn genomic sequencing
PURPOSE: Genomic sequencing (GS) for newborns may enable detection of conditions for which early knowledge can improve health outcomes. One of the major challenges hindering its broader application is the time it takes to assess the clinical relevance of detected variants and the genes they impact s...
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| Publicado no: | Genet Med |
|---|---|
| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5507765/ https://ncbi.nlm.nih.gov/pubmed/28079900 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2016.193 |
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