Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients
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Title
Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients
Authors
Keywords
Breast cancer, Mutation, <em class=EmphasisTypeItalic >BRCA1</em>, <em class=EmphasisTypeItalic >BRCA2</em>, <em class=EmphasisTypeItalic >HBOC</em>, <em class=EmphasisTypeItalic >CHEK 1100delC</em>, <em class=EmphasisTypeItalic >TP53 R337H</em>
Journal
BMC Medical Genetics
Volume 15, Issue 1, Pages -
Publisher
Springer Nature
Online
2014-05-15
DOI
10.1186/1471-2350-15-55
References
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Related references
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- Breast and Ovarian Cancer Risk and Risk Reduction in JewishBRCA1/2Mutation Carriers
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- Comprehensive molecular portraits of human breast tumours
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- (2011) Amy S. Clark et al. JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA
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- Detection of R337H, a germline TP53 mutation predisposing to multiple cancers, in asymptomatic women participating in a breast cancer screening program in Southern Brazil
- (2008) Edenir Inêz Palmero et al. CANCER LETTERS
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