Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancer.
Hum Mutat
; 42(3): 290-299, 2021 03.
Article
in En
| MEDLINE
| ID: mdl-33326660
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Ovarian Neoplasms
/
Breast Neoplasms
/
Hereditary Breast and Ovarian Cancer Syndrome
Type of study:
Etiology_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Female
/
Humans
Language:
En
Year:
2021
Type:
Article