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