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Article

Prenatal phenotypes and pregnancy outcomes of fetuses with recurrent 16p13.11 microduplications.

Medicine - 5 Jun 2026

Xu Tangfei, Yue Fagui, Ge Yao, Liu Ruizhi

Abstract excerpt

16p13.11 microduplication is a frequently observed chromosomal abnormality in newborns. However, prenatal reports for this chromosome microscopic imbalance are rare in clinical practice. This study aimed to provide a systematic summary of prenatal phenotypes for this genomic disorder. Between April 2019 and May 2023, 10 pregnant women underwent amniocentesis due to fetal ultrasound abnormalities, advanced...

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Share to Chromosomes, Human, Pair 16

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 42260801
DOI: 10.1097/MD.0000000000049059
PMCID: PMC13246041

Genes

ABCC1
ABCC6
MYH11
NDE1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

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