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Familial clustering of site-specific cancer risks associated with BRCA1 and BRCA2 mutations in the Ashkenazi Jewish population.
Proc Natl Acad Sci U S A. 2006 Mar 7;103(10):3770-4. doi: 10.1073/pnas.0511301103. Epub 2006 Feb 28.
Proc Natl Acad Sci U S A. 2006.
PMID: 16537453
Free PMC article.
The Jewish people: their ethnic history, genetic disorders and specific cancer susceptibility.
Kedar-Barnes I, Rozen P.
Kedar-Barnes I, et al.
Fam Cancer. 2004;3(3-4):193-9. doi: 10.1007/s10689-004-9544-0.
Fam Cancer. 2004.
PMID: 15516841
Review.
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Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I.
Toledano H, Goldberg Y, Kedar-Barnes I, Baris H, Porat RM, Shochat C, Bercovich D, Pikarsky E, Lerer I, Yaniv I, Abeliovich D, Peretz T.
Toledano H, et al. Among authors: kedar barnes i.
Fam Cancer. 2009;8(3):187-94. doi: 10.1007/s10689-008-9227-3. Epub 2008 Dec 20.
Fam Cancer. 2009.
PMID: 19101824
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Switching from tacrolimus to sirolimus halts the appearance of new sebaceous neoplasms in Muir-Torre syndrome.
Levi Z, Hazazi R, Kedar-Barnes I, Hodak E, Gal E, Mor E, Niv Y, Winkler J.
Levi Z, et al. Among authors: kedar barnes i.
Am J Transplant. 2007 Feb;7(2):476-9. doi: 10.1111/j.1600-6143.2006.01648.x. Epub 2007 Jan 4.
Am J Transplant. 2007.
PMID: 17229076
Free article.
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