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Oxford University Press

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Impaired replication dynamics at the FRA3B common fragile site

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Common chromosomal fragile site FRA16D mutation in cancer cells

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Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

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FRA3B Extends Over a Broad Region and Contains a Spontaneous HPV16 Integration Site: Direct Evidence for the Coincidence of Viral Integration Sites and Fragile Sites

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