Peretz T - Search Results

1

A deletion/insertion mutation in the BRCA2 gene in a breast cancer family: a possible role of the Alu-polyA tail in the evolution of the deletion.

Wang T, Lerer I, Gueta Z, Sagi M, Kadouri L, Peretz T, Abeliovich D. Wang T, et al. Among authors: peretz t. Genes Chromosomes Cancer. 2001 May;31(1):91-5. doi: 10.1002/gcc.1110. Genes Chromosomes Cancer. 2001. PMID: 11284040

2

The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals.

Struewing JP, Abeliovich D, Peretz T, Avishai N, Kaback MM, Collins FS, Brody LC. Struewing JP, et al. Among authors: peretz t. Nat Genet. 1995 Oct;11(2):198-200. doi: 10.1038/ng1095-198. Nat Genet. 1995. PMID: 7550349

3

[Genetic counseling for families at high cancer risk].

Sagi M, Heching N, Kadouri L, Abeliovich D, Zlotogora J, Bach G, Peretz T. Sagi M, et al. Among authors: peretz t. Harefuah. 1996 Apr 1;130(7):441-6, 504. Harefuah. 1996. PMID: 8707209 Hebrew.

4

Microsatellite instability and p53 mutations in therapy-related leukemia suggest mutator phenotype.

Ben-Yehuda D, Krichevsky S, Caspi O, Rund D, Polliack A, Abeliovich D, Zelig O, Yahalom V, Paltiel O, Or R, Peretz T, Ben-Neriah S, Yehuda O, Rachmilewitz EA. Ben-Yehuda D, et al. Among authors: peretz t. Blood. 1996 Dec 1;88(11):4296-303. Blood. 1996. PMID: 8943866 Free article.

5

[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.

6

The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women.

Abeliovich D, Kaduri L, Lerer I, Weinberg N, Amir G, Sagi M, Zlotogora J, Heching N, Peretz T. Abeliovich D, et al. Among authors: peretz t. Am J Hum Genet. 1997 Mar;60(3):505-14. Am J Hum Genet. 1997. PMID: 9042909 Free PMC article.

7

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.

8

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.

9

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.

10

Genetic testing of breast and ovarian cancer patients: clinical characteristics and hormonal risk modifiers.

Kaduri L, Gibs M, Hubert A, Sagi M, Heching N, Lerer I, Uziely B, Weinberg N, Abeliovich D, Peretz T. Kaduri L, et al. Among authors: peretz t. Eur J Obstet Gynecol Reprod Biol. 1999 Jul;85(1):75-80. doi: 10.1016/s0301-2115(98)00286-3. Eur J Obstet Gynecol Reprod Biol. 1999. PMID: 10428326

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