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- W121485229 endingPage "262" @default.
- W121485229 startingPage "247" @default.
- W121485229 abstract "X chromosome rearrangements usually convey clinical manifestations in the hemizygous males and are, thus, readily ascertained. They are found in all parts of the X chromosome and are associated with more than 20 disorders. Some of the rearrangements are the results of homologous recombination between low-copy repeats (LCRs) on the X chromosome or between large homologous regions on the X and Y chromosome, whereas others are caused by nonhomologous end-joining (NHEJ). For most large deletions associated with contiguous gene syndromes, the deletion breakpoints remain uncharacterized. The deletions, as well as inversions and duplications on the X chromosome, occur mainly in male germ cells, indicating intrachromatid or sister chromatid exchange as the underlying mechanism." @default.
- W121485229 created "2016-06-24" @default.
- W121485229 creator A5005383163 @default.
- W121485229 date "2007-11-10" @default.
- W121485229 modified "2023-09-25" @default.
- W121485229 title "X Chromosome Rearrangements" @default.
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