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Article

Prenatal diagnosis of congenital heart defect by genome-wide high-resolution SNP array.

Prenatal diagnosis - 1 Sept 2014

Liao Can, Li Ru, Fu Fang, Xie Guie, Zhang Yongling, Pan Min, Li Jian, Li Dongzhi

Abstract excerpt

OBJECTIVE: This study aimed to detect genomic imbalances in fetuses with congenital heart defect (CHD) by high-resolution single-nucleotide polymorphism (SNP) array. METHODS: A total of 99 fetuses with CHDs with or without other ultrasound anomalies (including structural anomalies and soft markers) but normal karyotypes were investigated using Affymetrix CytoScan HD array. RESULTS: Clinical significant copy...

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Source

Identifiers

PMID: 24718970
DOI: 10.1002/pd.4383

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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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