지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2016.6
- 수록면
- 1 - 9 (9page)
- DOI
- http://dx.doi.org/10.14449/jbd.2016.4.1.1
이용수
초록· 키워드
오류제보하기
Hereditary breast and ovarian cancer syndrome accounts for approximately 5% to 10% of breast or ovarian cancers, with which the high-penetrant BRCA1/2 genes have been associated. With the recent development of next-generation sequencing (NGS), germline mutation testing and its related medical and surgical management have been rapidly changing. In this review, we summarize the current status and perspectives of NGS testing for not only BRCA1/2 but also the other breast and ovarian cancer susceptibility genes.
목차
등록된 정보가 없습니다.
참고문헌 (62)
참고문헌 신청
Rich TA / 2015 / Hereditary breast cancer syndromes and genetic testing / J Surg Oncol 111:66~80
Carroll JC / 2008 / Hereditary breast and ovarian cancers / Can Fam Physician 54:1691~1692
Hall JM / 1990 / Linkage of early-onset familial breast cancer to chromosome 17q21 / Science 250:1684~1689
Miki Y / 1994 / A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1 / Science 266:66~71
Wooster R / 1994 / Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13 / Science 265:2088~2090
Carroll JC / 2008 / Hereditary breast and ovarian cancers / Can Fam Physician 54:1691~1692
Hall JM / 1990 / Linkage of early-onset familial breast cancer to chromosome 17q21 / Science 250:1684~1689
Miki Y / 1994 / A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1 / Science 266:66~71
Wooster R / 1994 / Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13 / Science 265:2088~2090
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