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Fundoscopy-directed genetic testing to re-evaluate negative whole exome sequencing results
BACKGROUND: Whole exome sequencing (WES) allows for an unbiased search of the genetic cause of a disease. Employing it as a first-tier genetic testing can be favored due to the associated lower incremental cost per diagnosis compared to when using it later in the diagnostic pathway. However, there a...
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| Publicado no: | Orphanet J Rare Dis |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6993391/ https://ncbi.nlm.nih.gov/pubmed/32000842 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-1312-1 |
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