Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications
<p>Abstract</p> <p>Background</p> <p>The 22q11.2 deletion syndrome is the most frequent genomic disorder with an estimated frequency of 1/4000 live births. The majority of patients (90%) have the same deletion of 3 Mb (Typically Deleted Region, TDR) that results from ab...
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| Main Authors: | , , , , |
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| Format: | Book |
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BMC,
2007-04-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |