Use of association studies to define genetic modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics (clinical),Oncology,Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10689-008-9181-0.pdf
Reference100 articles.
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2. Wooster R, Bignell G, Lancaster J, Swift S, Seal S, Mangion J, Collins N et al (1995) Identification of the breast cancer susceptibility gene BRCA2. Nature 378:789–791
3. Tavtigian SV, Simard J, Rommens J, Couch F, Shattuck-Eidens D, Neuhausen S, Merajver S et al (1996) The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds. Nat Genet 12:333–337
4. Easton DF, Ford D, Bishop DT (1995) Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast cancer linkage consortium. Am J Hum Genet 56:265–271
5. Ford D, Easton DF, Bishop DT, Narod SA, Goldgar DE (1994) Risks of cancer in BRCA1-mutation carriers. Breast cancer linkage consortium. Lancet 343:692–695
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