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Breast Cancer Screening and Diagnosis: A Synopsis

This booklet offers the present traits and practices in breast imaging. subject matters contain mammographic interpretation; breast ultrasound; breast MRI; administration of the symptomatic breast in younger, pregnant and lactating ladies; breast intervention with imaging pathological correlation; the postoperative breast and present and rising applied sciences in breast imaging. It emphasizes the significance of fostering a multidisciplinary procedure within the analysis and remedy of breast illnesses. that includes greater than 800 high-resolution pictures and showcasing contributions from prime specialists within the screening, prognosis and administration of the breast melanoma sufferer, Breast melanoma Screening and analysis is a invaluable source for radiologists, oncologists and surgeons.

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Hered Cancer Clin Pract. 2009;7(1):4. 143. Weischer M, et al. CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: meta-analyses of 26,000 patient cases and 27,000 controls. J Clin Oncol. 2008;26(4):542–8. 144. Adank MA, et al. CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women. J Med Genet. 2011; 48(12):860–3. 145. Offit K, Garber JE. Time to check CHEK2 in families with breast cancer? J Clin Oncol. 2008;26(4):519–20. 146. Bartkova J, et al. Aberrations of the MRE11-RAD50-NBS1 DNA damage sensor complex in human breast cancer: MRE11 as a candidate familial cancer-predisposing gene.

Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer. Cancer Res. 2011;71(6):2222–9. 178. Peterlongo P, et al. PALB2 germline mutations in familial breast cancer cases with personal and family history of pancreatic cancer. Breast Cancer Res Treat. 2011;126(3):825–8. 179. Southey MC, et al. A PALB2 mutation associated with high risk of breast cancer. Breast Cancer Res. 2010;12(6):R109. 180. Bogdanova N, et al. PALB2 mutations in German and Russian patients with bilateral breast cancer.

23. Shattuck-Eidens D, et al. BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing. JAMA. 1997;278(15):1242–50. 24. Kang HH, et al. Evaluation of models to predict BRCA germline mutations. Br J Cancer. 2006;95(7):914–20. 25. Barcenas CH, et al. Assessing BRCA carrier probabilities in extended families. J Clin Oncol. 2006;24(3):354–60. 26. James PA, et al. Optimal selection of individuals for BRCA mutation testing: a comparison of available methods.

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