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Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations
BACKGROUND: Hereditary cancer predisposition syndromes are responsible for approximately 5–10% of all diagnosed cancer cases. In the past, single-gene analysis of specific high risk genes was used for the determination of the genetic cause of cancer heritability in certain families. The application...
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| Publicado no: | BMC Cancer |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6547505/ https://ncbi.nlm.nih.gov/pubmed/31159747 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12885-019-5756-4 |
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