Modifiers of risk of hereditary breast and ovarian cancer
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Earth and Planetary Sciences,General Environmental Science
Link
http://www.nature.com/articles/nrc726.pdf
Reference77 articles.
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2. Nuemann, H. P. H. et al. Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel–Lindau disease. N. Engl. J. Med. 329, 1531–1538 (1993).
3. Wohllk, N. et al. Relevance of RET proto-oncogene mutations in sporadic medullary thyroid carcinoma. J. Clin. Endocrinol. Metab. 81, 3740–3745 (1996).
4. Aziz, S. et al. A genetic epidemiology study of carcinoma of the fallopian tube. Gynecol. Oncol. 80, 341–345 (2001).
5. Frank, T. S. et al. Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk. J. Clin. Oncol. 16, 2417–2425 (1998).
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