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Common fragile sites as targets for chromosome rearrangements
Martin F. Arlt et al.
DNA REPAIR (2006)
BRAF copy number gains in thyroid tumors detected by fluorescence in situ hybridization
R Ciampi et al.
ENDOCRINE PATHOLOGY (2005)
Dose-dependent generation of RET/PTC in human thyroid cells after in vitro exposure to γ-radiation:: A model of carcinogenic chromosomal rearrangement induced by ionizing radiation
CM Caudill et al.
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Chromosomal instability at common fragile sites in Seckel syndrome
AM Casper et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
The role of late/slow replication of the FRA16D in common fragile site induction
A Palakodeti et al.
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Molecular basis for expression of common and rare fragile sites
E Zlotorynski et al.
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Genetic alterations in cancer as a result of breakage at fragile sites
NC Popescu
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ATR regulates fragile site stability
AM Casper et al.
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A role for common fragile site induction in amplification of human oncogenes
A Hellman et al.
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RET rearrangements in radiation-induced papillary thyroid carcinomas: High prevalence of topoisomerase I sites at breakpoints and microhomology-mediated end joining in ELE1 and RET chimeric genes
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Breaksite batch mapping, a rapid method for assay and identification of DNA breaksites in mammalian cells
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CL Fenton et al.
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