Xp22.31 copy number variations in 87 fetuses: refined genotype-phenotype correlations by prenatal and postnatal follow-up
Abstract Background Xp22.31 deletion and duplication have been described in various studies, but different laboratories interpret pathogenicity differently. Objectives Our study aimed to refine the genotype-phenotype associations between Xp22.31 copy number variants in fetuses, with the aim of provi...
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Main Authors: | , , , , , , , , |
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Format: | Book |
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BMC,
2023-04-01T00:00:00Z.
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A1234.567 |
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Copy 1 | Available |