Risk of cancer at sites other than the breast in Swedish families eligible for BRCA1 or BRCA2 mutation testing-Reference-Cited by-同舟云学术

Risk of cancer at sites other than the breast in Swedish families eligible for BRCA1 or BRCA2 mutation testing

Published:2004-12 Issue:12 Volume:15 Page:1834-1841
ISSN:0923-7534
Container-title:Annals of Oncology
language:en
Short-container-title:Annals of Oncology

Author:

Lorenzo Bermejo J.,Hemminki K.

Publisher

Elsevier BV

Subject

Oncology,Hematology

Link

http://academic.oup.com/annonc/article-pdf/15/12/1834/830164/mdh474.pdf

Reference19 articles.

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3. Risks of cancer in BRCA1-mutation carriers;Ford;Breast Cancer Linkage Consortium. Lancet,1994

4. Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program;Brose;J Natl Cancer Inst,2002

5. Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer;Risch;Am J Hum Genet,2001

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4. Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma;Melanoma Research;2019-10

5. Hereditary and non-hereditary branches of family eligible for BRCA test: cancers in other sites;Hereditary Cancer in Clinical Practice;2017-05-25