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Article

Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes.

Archives of gynecology and obstetrics - 1 Nov 2017

Fu Fang, Deng Qiong, Lei Ting-Ying, Li Ru, Jing Xiang-Yi, Yang Xin, Liao Can

Abstract excerpt

PURPOSE: The present study aims to evaluate the utility of high-resolution single-nucleotide polymorphism (SNP) arrays in fetuses with ventricular septal defects (VSDs) with or without other structural anomalies but with normal karyotypes and to investigate the outcomes of cases of prenatal VSDs via clinical follow-up. METHODS: We analyzed 144 fetuses with VSDs and normal karyotypes using Affymetrix CytoScan HD...

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Share to Chromosome Disorders
Share to Chromosomes, Human, Pair 4

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gestational Age

Share to Heart Defects, Congenital

Share to Heart Septal Defects, Ventricular

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Source

Identifiers

PMID: 28905115
DOI: 10.1007/s00404-017-4518-2

Genes

AKAP10
EHMT1
ERCC4
FAT1
GJA5
LZTR1
NOTCH1
SKI
TBX1
ULK1
YWHAE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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