Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders
Abstract Background Structural rearrangements of the genome, which generally occur during meiosis and result in large-scale (> 1 kb) copy number variants (CNV; deletions or duplications ≥ 1 kb), underlie genomic disorders. Recurrent pathogenic CNVs harbor similar breakpoints in multiple unrelated...
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Format: | Book |
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BMC,
2021-06-01T00:00:00Z.
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A1234.567 |
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