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Volumn 133, Issue 3, 2012, Pages 1179-1190

Rare germline large rearrangements in the BRCA1/2 genes and eight candidate genes in 472 patients with breast cancer predisposition

(27)  Rouleau, E a   Jesson, B b   Briaux, A a   Nogues, C a   Chabaud, V b   Demange, L a   Sokolowska, J c   Coulet, F d   Barouk Simonet, E e   Bignon, Y J f   Bonnet, F e   Bourdon, V g   Bronner, M c   Caputo, S a   Castera, L h   Delnatte, C i   Delvincourt, C j   Fournier, J k   Hardouin, A l   Muller, D m   more..


Author keywords

BRCA1; BRCA2; Breast cancer predisposition; CGH array; Deletion; Duplication; Large rearrangements

Indexed keywords

3' UNTRANSLATED REGION; 5' UNTRANSLATED REGION; ADULT; ARTICLE; ATM GENE; BARD1 GENE; BREAST CANCER; BRIP1 GENE; CANCER PATIENT; CANCER SUSCEPTIBILITY; CHEK2 GENE; COMPARATIVE GENOMIC HYBRIDIZATION; DNA FLANKING REGION; EXPLORATORY RESEARCH; FAMILIAL CANCER; FEMALE; FRAMESHIFT MUTATION; FRANCE; GENE; GENE DELETION; GENE IDENTIFICATION; GENE MUTATION; GENE REARRANGEMENT; GENETIC CODE; GENETIC PREDISPOSITION; GENETIC SCREENING; GENOMICS; GERM LINE; HETEROZYGOTE; HUMAN; INCIDENCE; INTRON; MAJOR CLINICAL STUDY; NUCLEOTIDE SEQUENCE; OVARY CANCER; PALB2 GENE; PRIORITY JOURNAL; RAD50 GENE; RAD51 GENE; RAP80 GENE; TUMOR SUPPRESSOR GENE;

EID: 84863718085     PISSN: 01676806     EISSN: 15737217     Source Type: Journal    
DOI: 10.1007/s10549-012-2009-5     Document Type: Article
Times cited : (20)

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