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Title
RAD51B in Familial Breast Cancer
Authors
Keywords
Breast cancer, Haplotypes, Ovarian cancer, Introns, Variant genotypes, Genetic causes of cancer, Finnish people, Finland
Journal
PLoS One
Volume 11, Issue 5, Pages e0153788
Publisher
Public Library of Science (PLoS)
Online
2016-05-06
DOI
10.1371/journal.pone.0153788
References
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Related references
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- PON-P: Integrated predictor for pathogenicity of missense variants
- (2012) Ayodeji Olatubosun et al. HUMAN MUTATION
- Rare variants in XRCC2 as breast cancer susceptibility alleles: Table 1
- (2012) Florentine S Hilbers et al. JOURNAL OF MEDICAL GENETICS
- A Finnish founder mutation inRAD51D: analysis in breast, ovarian, prostate, and colorectal cancer: Table 1
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- (2012) Morten Källberg et al. Nature Protocols
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- (2011) Julie Johnson et al. BREAST CANCER RESEARCH AND TREATMENT
- RAD51C is a susceptibility gene for ovarian cancer
- (2011) Liisa M. Pelttari et al. HUMAN MOLECULAR GENETICS
- Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium†
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- The emerging landscape of breast cancer susceptibility
- (2007) Michael R Stratton et al. NATURE GENETICS
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