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Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations.
Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, Elstrodt F, van Duijn C, Bartels C, Meijers C, Schutte M, McGuffog L, Thompson D, Easton D, Sodha N, Seal S, Barfoot R, Mangion J, Chang-Claude J, Eccles D, Eeles R, Evans DG, Houlston R, Murday V, Narod S, Peretz T, Peto J, Phelan C, Zhang HX, Szabo C, Devilee P, Goldgar D, Futreal PA, Nathanson KL, Weber B, Rahman N, Stratton MR; CHEK2-Breast Cancer Consortium. Meijers-Heijboer H, et al. Among authors: peretz t. Nat Genet. 2002 May;31(1):55-9. doi: 10.1038/ng879. Epub 2002 Apr 22. Nat Genet. 2002. PMID: 11967536
Double heterozygotes for the Ashkenazi founder mutations in BRCA1 and BRCA2 genes.
Friedman E, Bar-Sade Bruchim R, Kruglikova A, Risel S, Levy-Lahad E, Halle D, Bar-On E, Gershoni-Baruch R, Dagan E, Kepten I, Peretz T, Lerer I, Wienberg N, Shushan A, Abeliovich AD. Friedman E, et al. Among authors: peretz t. Am J Hum Genet. 1998 Oct;63(4):1224-7. doi: 10.1086/302040. Am J Hum Genet. 1998. PMID: 9758598 Free PMC article. No abstract available.
The 8765delAG mutation in BRCA2 is common among Jews of Yemenite extraction.
Lerer I, Wang T, Peretz T, Sagi M, Kaduri L, Orr-Urtreger A, Stadler J, Gutman H, Abeliovich D. Lerer I, et al. Among authors: peretz t. Am J Hum Genet. 1998 Jul;63(1):272-4. doi: 10.1086/301924. Am J Hum Genet. 1998. PMID: 9634522 Free PMC article. No abstract available.
BRCA1 mutations in women with ovarian cancer.
Shushan A, Abeliovich D, Peretz T, Weinberg N, Paltiel O. Shushan A, et al. Among authors: peretz t. JAMA. 1997 Mar 26;277(12):963. JAMA. 1997. PMID: 9091664 No abstract available.
[Inherited breast cancer].
Kaduri L, Heshing N, Abeliovich D, Peretz T. Kaduri L, et al. Among authors: peretz t. Harefuah. 1996 Nov 15;131(10):418-21. Harefuah. 1996. PMID: 8981821 Review. Hebrew. No abstract available.
307 results