Large BRCA1 and BRCA2 genomic rearrangements in Danish high risk breast-ovarian cancer families

Breast Cancer Research and Treatment

Volumn 115, Issue 2, 2009, Pages 315-323

  Hansen, Thomas V O ^a   Jønson, Lars ^a   Albrechtsen, Anders ^b   Andersen, Mette K ^a   Ejlertsen, Bent ^a   Nielsen, Finn C ^a  

^a Rigshospitalet   (Denmark)

^b UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

BRCA1; BRCA2; Breakpoint; Danish founder mutation; Deletion; Duplication; MLPA; SNP array

Indexed keywords

BRCA1 PROTEIN; BRCA2 PROTEIN;

ADULT; ARTICLE; BREAST CANCER; CANCER PATIENT; CANCER RISK; CHROMOSOME 17; CONTROLLED STUDY; DENMARK; EXON; FEMALE; GENE DELETION; GENE DUPLICATION; GENE MUTATION; GENE REARRANGEMENT; GENE SEQUENCE; HIGH RISK POPULATION; HUMAN; MAJOR CLINICAL STUDY; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; NUCLEOTIDE SEQUENCE; OVARY CANCER; PRIORITY JOURNAL; RISK ASSESSMENT; SINGLE NUCLEOTIDE POLYMORPHISM;

BASE SEQUENCE; BREAST NEOPLASMS; DENMARK; FEMALE; FOUNDER EFFECT; GENE REARRANGEMENT; GENES, BRCA1; GENES, BRCA2; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; OVARIAN NEOPLASMS; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS;

EID: 67349101217     PISSN: 01676806     EISSN: 15737217     Source Type: Journal    
DOI: 10.1007/s10549-008-0088-0     Document Type: Article

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