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Family-specific, novel, deleterious germline variants provide a rich resource to identify genetic predispositions for BRCAx familial breast cancer.
BMC Cancer. 2014 Jun 26;14:470. doi: 10.1186/1471-2407-14-470.
BMC Cancer. 2014.
PMID: 24969172
Free PMC article.
Two PALB2 germline mutations found in both BRCA1+ and BRCAx familial breast cancer.
Downs B, Kim YC, Xiao F, Snyder C, Chen P, Fleissner EA, Becirovic D, Wen H, Sherman S, Cowan KH, Lynch HT, Wang SM.
Downs B, et al. Among authors: fleissner ea.
Breast Cancer Res Treat. 2015 May;151(1):219-24. doi: 10.1007/s10549-015-3358-7. Epub 2015 Apr 2.
Breast Cancer Res Treat. 2015.
PMID: 25833210
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Single-base LOH can be used as Specific Marker to Classify BRCAx Familial Breast Cancer into More Homogenous Subtypes.
Downs B, Xiao F, Kim YC, Chen PX, Huang D, Fleissner EA, Cowan K, Wang SM.
Downs B, et al. Among authors: fleissner ea.
Breast J. 2017 Jul;23(4):479-481. doi: 10.1111/tbj.12777. Epub 2017 Jan 24.
Breast J. 2017.
PMID: 28117528
Free PMC article.
No abstract available.
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Multicenter breast cancer collaborative registry.
Sherman S, Shats O, Fleissner E, Bascom G, Yiee K, Copur M, Crow K, Rooney J, Mateen Z, Ketcham MA, Feng J, Sherman A, Gleason M, Kinarsky L, Silva-Lopez E, Edney J, Reed E, Berger A, Cowan K.
Sherman S, et al.
Cancer Inform. 2011;10:217-26. doi: 10.4137/CIN.S7845. Epub 2011 Aug 31.
Cancer Inform. 2011.
PMID: 21918596
Free PMC article.
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