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Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2.
Mutat Res. 2006 Oct 10;601(1-2):191-201. doi: 10.1016/j.mrfmmm.2006.07.003. Epub 2006 Aug 21.
Mutat Res. 2006.
PMID: 16920162
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
Levitus M, Waisfisz Q, Godthelp BC, de Vries Y, Hussain S, Wiegant WW, Elghalbzouri-Maghrani E, Steltenpool J, Rooimans MA, Pals G, Arwert F, Mathew CG, Zdzienicka MZ, Hiom K, De Winter JP, Joenje H.
Levitus M, et al. Among authors: elghalbzouri maghrani e.
Nat Genet. 2005 Sep;37(9):934-5. doi: 10.1038/ng1625. Epub 2005 Aug 21.
Nat Genet. 2005.
PMID: 16116423
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Increased DNA damage sensitivity of Cornelia de Lange syndrome cells: evidence for impaired recombinational repair.
Vrouwe MG, Elghalbzouri-Maghrani E, Meijers M, Schouten P, Godthelp BC, Bhuiyan ZA, Redeker EJ, Mannens MM, Mullenders LH, Pastink A, Darroudi F.
Vrouwe MG, et al. Among authors: elghalbzouri maghrani e.
Hum Mol Genet. 2007 Jun 15;16(12):1478-87. doi: 10.1093/hmg/ddm098. Epub 2007 Apr 27.
Hum Mol Genet. 2007.
PMID: 17468178
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Does tumorigenesis select for or against mutations of the DNA repair-associated genes BRCA2 and MRE11?: considerations from somatic mutations in microsatellite unstable (MSI) gastrointestinal cancers.
van der Heijden MS, Brody JR, Elghalbzouri-Maghrani E, Zdzienicka MZ, Kern SE.
van der Heijden MS, et al. Among authors: elghalbzouri maghrani e.
BMC Genet. 2006 Jan 17;7:3. doi: 10.1186/1471-2156-7-3.
BMC Genet. 2006.
PMID: 16417627
Free PMC article.
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