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Article

Genetic Analysis of a Fetus with 14q11.2 Microdeletion in Ultrasound Abnormalities.

Clinical laboratory - 1 Sept 2024

Zhang Yan, Lin Kun, Zeng Li-Na, Lin Li, Dong Xian, Wang Jing-Jing, Chen Huang-Hui

Abstract excerpt

BACKGROUND: This study aimed to explore the genetic basis of a fetus with ultrasound indicating a thickening of the nuchal translucency (NT) and a choroid plexus cyst. METHODS: Fetal amniotic fluid and peripheral blood were collected for a G-banding karyotype analysis and single nucleotide polymorphism array (SNP-array) detection. RESULTS: The chromosome karyotypes of the fetus and its parents were normal....

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Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 14

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fetal Growth Retardation

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Source

Identifiers

PMID: 39257112
DOI: 10.7754/Clin.Lab.2024.240335

Provenance

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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