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: Huamei Hu (Author), Yulin Huang (Author), Renke Hou (Author), Huanhuan Xu (Author), Yalan Liu (Author), Xueqian Liao (Author), Juchun Xu (Author), Lupin Jiang (Author), Dan Wang (Author)
Format: Book
Published: BMC, 2023-04-01T00:00:00Z.
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