Copy Number Variations (CNVs) Account for 10.8% of Pathogenic Variants in Patients Referred for Hereditary Cancer Testing.
Cancer Genomics Proteomics
; 20(5): 448-455, 2023.
Article
in En
| MEDLINE
| ID: mdl-37643779
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Ovarian Neoplasms
/
DNA Copy Number Variations
Type of study:
Prognostic_studies
Limits:
Female
/
Humans
Language:
En
Journal:
Cancer Genomics Proteomics
Journal subject:
BIOQUIMICA
/
GENETICA MEDICA
/
NEOPLASIAS
Year:
2023
Document type:
Article