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Germline and tumor BRCA1/2 mutations in Chinese high grade serous ovarian cancer patients
BACKGROUND: Studies on the prevalence of BRCA1/2 mutations in ovarian cancer mainly focused on germline single-nucleotide variant (SNV)/insertion/deletion (indel). The status of large genomic rearrangement (LRG) and somatic mutation were poorly investigated. METHODS: Paired blood and tumor DNA from...
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| Publicado no: | Ann Transl Med |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
AME Publishing Company
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8039691/ https://ncbi.nlm.nih.gov/pubmed/33850850 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm-20-6827 |
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