Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication
Abstract Background Chromosomal 16p11.2 deletions and duplications are genomic disorders which are characterized by neurobehavioral abnormalities, obesity, congenital abnormalities. However, the prenatal phenotypes associated with 16p11.2 copy number variations (CNVs) have not been well characterize...
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| Main Authors: | , , , , |
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| Format: | Book |
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BMC,
2024-07-01T00:00:00Z.
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A1234.567 |
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