Загрузка...
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...
Сохранить в:
| Опубликовано в: : | Eur J Hum Genet |
|---|---|
| Главные авторы: | , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Nature Publishing Group
2017
|
| Предметы: | |
| Online-ссылка: | 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 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|