Kadouri E - Search Results

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Association of the C677T polymorphism in the MTHFR gene with breast and/or ovarian cancer risk in Jewish women.

Gershoni-Baruch R, Dagan E, Israeli D, Kasinetz L, Kadouri E, Friedman E. Gershoni-Baruch R, et al. Among authors: kadouri e. Eur J Cancer. 2000 Dec;36(18):2313-6. doi: 10.1016/s0959-8049(00)00306-3. Eur J Cancer. 2000. PMID: 11094304

Association of the I1307K APC mutation with hereditary and sporadic breast/ovarian cancer: more questions than answers.

Gershoni-Baruch R, Patael Y, Dagan, Figer A, Kasinetz L, Kadouri E, Bruchim Bar Sade R, Friedman E. Gershoni-Baruch R, et al. Among authors: kadouri e. Br J Cancer. 2000 Jul;83(2):153-5. doi: 10.1054/bjoc.2000.1248. Br J Cancer. 2000. PMID: 10901363 Free PMC article.

Prenatal diagnosis of X-linked hyper-IGM syndrome by direct detection of mutation Q220X in the CD40L gene using PCR-mediated site directed mutagenesis.

Jayoussi-Assalia R, Etzioni A, Notarangelo LD, Brill-Zamir R, Kasinetz L, Kadouri E, Gershoni-Baruch R. Jayoussi-Assalia R, et al. Among authors: kadouri e. Prenat Diagn. 2000 Oct;20(10):822-3. doi: 10.1002/1097-0223(200010)20:10<822::aid-pd935>3.0.co;2-k. Prenat Diagn. 2000. PMID: 11038461

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