학술논문

Association of recurrent mutations in BRCA1, BRCA2, RAD51C, PALB2, and CHEK2 with the risk of borderline ovarian tumor
Document Type
Article
Source
In: Hereditary Cancer in Clinical Practice. (Hereditary Cancer in Clinical Practice, December 2022, 20(1))
Subject
Language
English
ISSN
18974287
17312302