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Article

Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication.

BMC pregnancy and childbirth - 22 Jul 2024

Yue Fagui, Hao Mengzhe, Jiang Dandan, Liu Ruizhi, Zhang Hongguo

Abstract excerpt

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 characterized. This study aimed to provide an elaborate summary of intrauterine phenotypic features for these genomic disorders....

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Identifiers

PMID: 39039444
DOI: 10.1186/s12884-024-06702-w
PMCID: PMC11265082

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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