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Whole-exome sequencing of Finnish hereditary breast cancer families
A remarkable proportion of factors causing genetic predisposition to breast cancer (BC) are unknown in non-BRCA1/2 families. Exome sequencing was performed for 13 high-risk Finnish hereditary breast and/or ovarian cancer (HBOC) families to detect variants contributing to BC susceptibility. After fil...
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| Publicat a: | Eur J Hum Genet |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5159774/ https://ncbi.nlm.nih.gov/pubmed/27782108 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2016.141 |
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