A de novo 10q11.23q22.1 deletion detected by whole genome mate-pair sequencing: a case report
Abstract Background Interstitial deletions of chromosome band 10q11-q22 was a genomic disorder distinguished by developmental delay, congenital cleft palate and muscular hypotonia. The phenotypes involved were heterogeneous, hinge on the variable breakpoints and size. Case presentation Here, we pres...
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Main Authors: | , , , , , , , , , , , , |
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Format: | Book |
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BMC,
2021-05-01T00:00:00Z.
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A1234.567 |
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